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PACE-4-AUTOMATIC RIA GAMMA-COUTER

K802578 Class I Traditional
Decision Date
1980-12-18
Sponsor / Applicant
Philips Medical Systems (Cleveland), Inc.

Technical Specification

510(k) Submission ID K802578
Product Code JJJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2320
Decision Date 1980-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACE-4-AUTOMATIC RIA GAMMA-COUTER received FDA 510(k) clearance under submission number K802578, sponsored by Philips Medical Systems (Cleveland), 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 1980-12-18.

Classification & Regulation

This clearance is catalogued under FDA product code JJJ and 21 CFR 862.2320, within the Clinical Chemistry review panel as a Class I device.