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MONITOR, LIQ. CHROMATOGRAPHY LC-15 UV

K771156 Class I Traditional
Decision Date
1977-08-02
Sponsor / Applicant
The Perkin-Elmer Corp.

Technical Specification

510(k) Submission ID K771156
Product Code KIE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2260
Decision Date 1977-08-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MONITOR, LIQ. CHROMATOGRAPHY LC-15 UV received FDA 510(k) clearance under submission number K771156, sponsored by The Perkin-Elmer 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 1977-08-02.

Classification & Regulation

This clearance is catalogued under FDA product code KIE and 21 CFR 862.2260, within the Clinical Chemistry review panel as a Class I device.