← Product Code [ILY](/productcode/ILY) · K053376

# CHUNG CHENG FAR INFRARED RAY HEALTHFUL LAMP (OR MEDICAL FIR RADIATOR), MODEL CH-8810 (K053376)

_Chung Cheng Electric Heating Co., Ltd. · ILY · Feb 16, 2006 · Physical Medicine · SESE_

**Canonical URL:** https://fda-staging.innolitics.com/device/K053376

## Device Facts

- **Applicant:** Chung Cheng Electric Heating Co., Ltd.
- **Product Code:** [ILY](/productcode/ILY.md)
- **Decision Date:** Feb 16, 2006
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 890.5500
- **Device Class:** Class 2
- **Review Panel:** Physical Medicine
- **Attributes:** Therapeutic

## Indications for Use

The "CHUNG CHENG " Far Infrared Ray healthful Lamp (« Medical FIR Radiator) Model #CH-8810 may be used for the temporary relief of minor muscle and joint pain and stiffness. the temporary relief of joint pain associated with arthritis, the temporary increase in local circulation where applied, and relaxation of muscles. In addition, the lamp may also help muscle spasms, minor sprains and strains, and minor muscular back pain.

## Device Story

The Chung Cheng Model #CH-8810 is a far infrared (FIR) heating lamp used for topical heat therapy. It utilizes an automatic control temperature ceramic semiconductor to emit infrared radiation in the 4 to 14-micron spectrum. The device operates on 120Vac power at 800W. It is intended for use in clinical or home settings to provide temporary relief from musculoskeletal pain, stiffness, and spasms, and to promote local circulation and muscle relaxation. The healthcare provider or patient positions the lamp to direct heat to the affected body area. The device's thermal output is intended to provide symptomatic relief for minor injuries and chronic conditions like arthritis.

## Clinical Evidence

Bench testing only. The device conforms to IEC 60601-1 (electrical safety) and IEC 60601-1-2 (electromagnetic compatibility) standards.

## Technological Characteristics

Far infrared heating lamp; emission spectrum 4-14 microns; 120Vac power source; 800W output; automatic control temperature ceramic semiconductor; conforms to IEC 60601-1 and IEC 60601-1-2.

## Regulatory Identification

An infrared lamp is a device intended for medical purposes that emits energy at infrared frequencies (approximately 700 nanometers to 50,000 nanometers) to provide topical heating.

## Special Controls

*Classification.* Class II (special controls). The device, when it is an infrared therapeutic heating lamp, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 890.9.

## Predicate Devices

- FIRARD II/ TDP LAMP ([K960036](/device/K960036.md))

## Submission Summary (Full Text)

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## 510(K) SUMMARY

K053761/2

FEB 1 6 2000

nis summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA and 21 CFR §807.92

## 1. Submitter's Name: CHUNG CHENG ELECTRIC HEATING CO., LTD.

- no. 39 huan kung RD., Yung Kang Industrial Address: area, yung kang city, tainan hsien, taiwan +886-6-2314078 Phone: +886-6-2330916 Fax: Mr. C.T. Chang/President Contact:
- 2. Device Name :

"CHUNG CHENG " Far Infrared Ray healthful Lamp Trade Name: (or Medical FIR Radiator) Model #CH-8810 Common Name: Infrared Heating Lamp

Classification name Lamp, Infrared

"CHUNG CHENG " Far Infrared Ray healthful Lamp (or 2 DEVICE CLASS Medical FIR Radiator) Model #CH-8810 have been classified as Requlatory Class: II Product Code: ILY Panel : Physical Medicine Requlation Number: 21CFR 890.5500

## The predicate device is the 4. Predicate Device: · FIRARD II/ TDP LAMP (K960036) marketed by HELIO

MEDICAL SUPPLIES, INC.

5. Device Description: The "CHUNG CHENG " Far Infrared Ray healthful Lamp (or Medical FIR Radiator) Model #CH-8810 can be used to emit topical heating to the body of human. The device make use of a "All In One" Automatic control Temperature Ceramic Semiconductor. Emission spectrum ranges from 4 to 14 microns. The device uses 120Vac as power source & 800W . it meets the related requirement of IEC 60601-1 Electrical Safety.

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K053376 2/2

6. Intended Use: The "CHUNG CHENG " Far Infrared Ray healthful Lamp (« Medical FIR Radiator) Model #CH-8810 may be used for the temporary relief of minor muscle and joint pain and stiffness. the temporary relief of joint pain associated with arthritis, the temporary increase in local circulation where applied, and relaxation of muscles. In addition, the lamp may also help muscle spasms, minor sprains and strains, and minor muscular back pain.

- 7. Performance The device conforms to applicable standards includes IEC Summary: 60601-1, IEC 60601-1-2 & related standards ---- etc.
- 8. Conclusions:

The "CHUNG CHENG " Far Infrared Ray healthful Lamp (or Medical FIR Radiator) Model #CH-8810 has the same intended use and similar technological characteristics as the FIRARD II/ TDP LAMP (K960036) marketed by HELIO MEDICAL SUPPLIES, INC.. Moreover, bench testing contained in this submission demonstrate that any differences in their technological characteristics do not raise any new questions of safety or effectiveness. Thus, the "CHUNG CHENG " Far Infrared Ray healthful Lamp (or Medical FIR Radiator) Model #CH-8810 is substantially equivalent to the predicate devices.

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DEPARTMENT OF HEALTH & HUMAN SERVICES

Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo features a stylized eagle with three stripes forming its body and wings. The eagle is positioned within a circle of text that reads "DEPARTMENT OF HEALTH AND HUMAN SERVICES · USA".

Public Health Service

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

FEB 1 6 2006

Chung Cheng Electric Heating Co., Ltd. c/o Ms. Jennifer Reich Harvest Consulting Corp. 2904 N. Boldt Drive Flagstaff, Arizona 86001

Re: K053376

R05370
Trade/Device Name: "CHUNG CHENG" Far Infrared Ray healthful Lamp (or Medical FIR Radiator) Model #CH-8810

Regulation Number: 21 CFR 890.5500 Regulation Name: Infrared lamp Regulatory Class: II Product Code: ILY Dated: January 26, 2006 Received: February 6, 2006

Dear Ms. Reich:

We have reviewed your Section 510(k) premarket notification of intent to market the device w oneve reviewed your betermined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate for about in to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, de nees mat have been reauire approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The r ou may, merers, mains of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it if your device to such additional controls. Existing major regulations affecting your device can may or babyer to back as a sateral Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Please be advised that FDA's issuance of a substantial equivalence determination does not mean r read o o a mode a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as sct Errth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic form in and quarty of brovisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

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Page 2 - Ms. Reich

This letter will allow you to begin marketing your device as described in your Section 510(k) This letter will anow you to oegin maneting your antial equivalence of your device to a legally premarket nothleadon: The PDF miaing of basification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please If you desire specific advice for your ac not on one of on the regulation entitled, connact the Office of Compullion in (21 m (21 CFR Part 807.97). You may obtain Missionaliding by reference to premance notifications in the Act from the Division of Small other general information on your response Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html

Sincerely yours,

Hubert Lemmens

Mark N. Melkerson Acting Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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## Indications for Use

510(k) Number (if known): K 05 3 3 76

Device Name: "CHUNG CHENG " Far Infrared Ray healthful Lamp
Device Name: "CHUNG CHEVE Barlieter) Model #CH-8810 CHONG ORENO ORDERS Model #CH-8810 (or Medical PIX Raulars)
CHUNG CHENG ELECTRIC HEATING CO., LTD.

Indications For Use:

The device may be used for the temporary relief of minor muscle and joint pain a
rther and the first and the taming secsioned with arthritis, the temporar The device may be used for the temporary rollor with atthritis, the temporary stiffness, the temporary relier of joint punt purcessation of muscles. In addition
increase in local circulation where applied, and relaxation and minor increase in local circulation where applied, and really and strains, and minor muscular back pain.

| Prescription Use<br>(Part 21 CFR 801 Subpart D) | AND/OR | Over-The-Counter Use<br>(21 CFR 807 Subpart C) | V |
|-------------------------------------------------|--------|------------------------------------------------|---|
|-------------------------------------------------|--------|------------------------------------------------|---|

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEED

Concurrence of CDRH, Office of Device Evaluation (ODE)

(Division Sign-Off)

Division of General, Restorative,  
and Neurological Devices

Page 1

510(k) Number__________

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