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PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP

K935666 Class I Traditional
Decision Date
1994-04-26
Sponsor / Applicant
The Perkin-Elmer Corp.

Technical Specification

510(k) Submission ID K935666
Product Code KIE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2260
Decision Date 1994-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP received FDA 510(k) clearance under submission number K935666, 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 1994-04-26.

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.