ERBOTOM ICC 350

K933002 · Erbe USA, Inc. · GEI · Mar 9, 1994 · General, Plastic Surgery

Device Facts

Record IDK933002
Device NameERBOTOM ICC 350
ApplicantErbe USA, Inc.
Product CodeGEI · General, Plastic Surgery
Decision DateMar 9, 1994
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 878.4400
Device ClassClass 2

Device Story

The Erbotom ICC 350 is an electrosurgical unit designed for use in surgical procedures. It functions by delivering high-frequency electrical current to tissue to achieve cutting and coagulation. Operated by surgeons or trained clinical staff in an operating room environment, the device transforms electrical energy into thermal effects at the surgical site. The output is controlled by the user to manage tissue interaction, facilitating surgical incision and hemostasis. The device benefits patients by providing precise tissue management during various surgical interventions.

Clinical Evidence

No clinical data provided; device cleared based on substantial equivalence to pre-amendment predicate devices.

Technological Characteristics

Electrosurgical generator; high-frequency electrical output for cutting and coagulation; Class II device.

Regulatory Classification

Identification

An electrosurgical cutting and coagulation device and accessories is a device intended to remove tissue and control bleeding by use of high-frequency electrical current.

Submission Summary (Full Text)

{0} [LOGO] DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service MAR 9 1994 Food and Drug Administration 1390 Piccard Drive Rockville MD 20850 Mr. Michael A. Clark Erbe USA, Inc. c/o South East Regulatory Associates 775 Oxford Hall Drive Lawrenceville, Georgia 30244 Re: K933002/S3 Erbotom ICC 350 Regulatory Class: II Dated: March 2, 1994 Received: March 2, 1994 Dear Mr. Clark: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments. You may, therefore, market the device, subject to the general controls provisions of the Federal Food, Drug, and Cosmetic Act (Act). The general controls provisions of the Act include requirements for registration, listing of devices, good manufacturing practice, and labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval) it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. In addition, the Food and Drug Administration (FDA) may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under the Radiation Control for Health and Safety Act of 1968, or other Federal Laws or Regulations. This letter immediately will allow you to begin marketing your device as described. An FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and permits your device to proceed to the market, but it does not mean that FDA approves your device. Therefore, you may not promote or in any way represent your device or its labeling as being approved by FDA. If you desire specific advice on the labeling for your device, please contact the Office of / {1} Page 2 - Mr. Michael A. Clark at (301) 594-4639. Other general information on your responsibilities under the Act, may be obtained from the Division of Small Manufacturers Assistance at their toll free number (800) 638-2041 or at (301) 443-6597. Sincerely yours, Paul R. Beninger, M.D. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health 2
Innolitics
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