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SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR

K962762 Class I Traditional
Decision Date
1996-08-16
Sponsor / Applicant
Biotraces, Inc.

Technical Specification

510(k) Submission ID K962762
Product Code JJJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2320
Decision Date 1996-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SEQUENTIAL SAMPLE MULTI-PHOTON DETECTOR received FDA 510(k) clearance under submission number K962762, sponsored by Biotraces, 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 1996-08-16.

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.