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KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KIT

K896440 Class I Traditional
Decision Date
1990-02-16
Sponsor / Applicant
Kenlor Industries, Inc.

Technical Specification

510(k) Submission ID K896440
Product Code JIR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1645
Decision Date 1990-02-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KIT received FDA 510(k) clearance under submission number K896440, sponsored by Kenlor Industries, 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 1990-02-16.

Classification & Regulation

This clearance is catalogued under FDA product code JIR and 21 CFR 862.1645, within the Clinical Chemistry review panel as a Class I device.