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MODEL LC-85 UV DETECTOR

K810304 Class I Traditional
Decision Date
1981-02-25
Sponsor / Applicant
The Perkin-Elmer Corp.

Technical Specification

510(k) Submission ID K810304
Product Code LDM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2260
Decision Date 1981-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL LC-85 UV DETECTOR received FDA 510(k) clearance under submission number K810304, 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 1981-02-25.

Classification & Regulation

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