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UNITEST-POTASSIUM

K812677 Class II Traditional
Decision Date
1981-10-02
Sponsor / Applicant
Biodynamics Corp.

Technical Specification

510(k) Submission ID K812677
Product Code CEJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1600
Decision Date 1981-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNITEST-POTASSIUM received FDA 510(k) clearance under submission number K812677, sponsored by Biodynamics Corp.. 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 1981-10-02.

Classification & Regulation

This clearance is catalogued under FDA product code CEJ and 21 CFR 862.1600, within the Clinical Chemistry review panel as a Class II device.