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FERMCOTEST CREATININE TEST REAGENT

K822118 Class II Traditional
Decision Date
1982-09-30
Sponsor / Applicant
Fermco Biochemics, Inc.

Technical Specification

510(k) Submission ID K822118
Product Code CGX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1225
Decision Date 1982-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FERMCOTEST CREATININE TEST REAGENT received FDA 510(k) clearance under submission number K822118, sponsored by Fermco Biochemics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1982-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code CGX and 21 CFR 862.1225, within the Clinical Chemistry review panel as a Class II device.