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TOTAL PROTEIN REAGENT

K890317 Class II Traditional
Decision Date
1989-03-08
Sponsor / Applicant
Medical Analysis Systems, Inc.

Technical Specification

510(k) Submission ID K890317
Product Code CEK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1635
Decision Date 1989-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL PROTEIN REAGENT received FDA 510(k) clearance under submission number K890317, sponsored by Medical Analysis Systems, 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 1989-03-08.

Classification & Regulation

This clearance is catalogued under FDA product code CEK and 21 CFR 862.1635, within the Clinical Chemistry review panel as a Class II device.