BETA HCG CONTROL LEVEL 1 BETA HCG CONTROL LEVEL 2 BETA HCG CONTROL LEVEL 3 BETA HCG CALIBRATION VERIFICATION CONTROLS LE

K121237 · Cliniqa Corporation · JJX · May 18, 2012 · Clinical Chemistry

Device Facts

Record IDK121237
Device NameBETA HCG CONTROL LEVEL 1 BETA HCG CONTROL LEVEL 2 BETA HCG CONTROL LEVEL 3 BETA HCG CALIBRATION VERIFICATION CONTROLS LE
ApplicantCliniqa Corporation
Product CodeJJX · Clinical Chemistry
Decision DateMay 18, 2012
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 862.1660
Device ClassClass 1

Indications for Use

Cliniqa Beta HCG Control Level 1, Cliniqa Beta HCG Control Level 2, Cliniqa Beta HCG Control Level 3, are assayed quality control materials used to monitor the precision of Beta HCG assays. Cliniga Beta HCG Calibration Verification Controls, Levels 1, 2, and 3 are assayed quality control materials used to monitor the precision of Beta HCG assays.

Device Story

Assayed quality control materials; human serum-based with purified human antigens, stabilizers, and preservatives. Used to monitor precision of Beta HCG assays. Ready-to-use liquid form; no reconstitution or freezing required. Used by laboratory personnel to verify assay performance; provides mean and expected range for specific lots. Stability: 3 years shelf life at 2-8°C; 30-day open-vial stability at 2-8°C. Benefits patient by ensuring accuracy and reliability of clinical Beta HCG test results.

Clinical Evidence

No clinical data. Evidence consists of bench testing, including value assignment studies and real-time/accelerated stability testing to support shelf-life and open-vial claims.

Technological Characteristics

Liquid quality control material; human serum matrix with added buffers, stabilizers, and purified human hormones. Storage at 2-8°C. Value assignment derived from representative lot analysis using reagents and calibrators standardized against NIBSC 75/589.

Indications for Use

Indicated for use as assayed quality control materials to monitor the precision of Beta HCG assays in clinical laboratory settings.

Regulatory Classification

Identification

A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls.

Submission Summary (Full Text)

{0} # Decision Summary Statement for the Record, k121237 This 510(k) was reviewed under OIVD’s Pilot Triage Program. This program represents an internal workload management tool intended to reduce internal FDA review resources for 510(k) applications that are of good quality upon receipt by FDA. The information in the 510(k) is complete and supports a substantial equivalence (SE) determination. Please refer to the applicant’s 510(k) summary for a summary of the information that supports this SE determination.
Innolitics

Panel 1

/
Ready

Predicate graph will load when search results are available.

Embedding visualization will load when search results are available.

PDF viewer will load when search results are available.

Loading panels...

Select an item from Submissions

Click any panel, subpart, regulation, product code, or device to see details here.

Section Matches

Results will appear here.

Product Code Matches

Results will appear here.

Special Control Matches

Results will appear here.

Loading collections...