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CREATININE REAGENT SET

K841070 Class II Traditional
Decision Date
1984-05-01
Sponsor / Applicant
Medical Specialties, Inc.

Technical Specification

510(k) Submission ID K841070
Product Code JFY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1225
Decision Date 1984-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CREATININE REAGENT SET received FDA 510(k) clearance under submission number K841070, sponsored by Medical Specialties, 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 1984-05-01.

Classification & Regulation

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