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LUMINESCENCE PHOTOMETER 100 SERIES

K810736 Class I Traditional
Decision Date
1981-03-31
Sponsor / Applicant
Sai Technology

Technical Specification

510(k) Submission ID K810736
Product Code JJQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2300
Decision Date 1981-03-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LUMINESCENCE PHOTOMETER 100 SERIES received FDA 510(k) clearance under submission number K810736, sponsored by Sai Technology. 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 1981-03-31.

Classification & Regulation

This clearance is catalogued under FDA product code JJQ and 21 CFR 862.2300, within the Clinical Chemistry review panel as a Class I device.