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POTASSIUM QVET

K943026 Class II Traditional
Decision Date
1994-12-09
Sponsor / Applicant
Prisma Systems

Technical Specification

510(k) Submission ID K943026
Product Code CEJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1600
Decision Date 1994-12-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POTASSIUM QVET received FDA 510(k) clearance under submission number K943026, sponsored by Prisma Systems. 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 1994-12-09.

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.