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UVMAX KINETIC MICROPLATE READER

K881803 Class I Traditional
Decision Date
1988-05-31
Sponsor / Applicant
Molecular Devices Corp.

Technical Specification

510(k) Submission ID K881803
Product Code JJQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2300
Decision Date 1988-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UVMAX KINETIC MICROPLATE READER received FDA 510(k) clearance under submission number K881803, sponsored by Molecular Devices 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 1988-05-31.

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.