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PERSONALLAB AUTOMATED MICROPLATE ANALYZER

K971761 Class I Traditional
Decision Date
1997-07-22
Sponsor / Applicant
Biochem Immunosystems (U.S.), Inc.

Technical Specification

510(k) Submission ID K971761
Product Code JJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2160
Decision Date 1997-07-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERSONALLAB AUTOMATED MICROPLATE ANALYZER received FDA 510(k) clearance under submission number K971761, sponsored by Biochem Immunosystems (U.S.), 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 1997-07-22.

Classification & Regulation

This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.