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MULTICHEM LDH-L REAGENT

K872010 Class II Traditional
Decision Date
1987-06-11
Sponsor / Applicant
Simmler, Inc.

Technical Specification

510(k) Submission ID K872010
Product Code CFJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1440
Decision Date 1987-06-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTICHEM LDH-L REAGENT received FDA 510(k) clearance under submission number K872010, sponsored by Simmler, 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 1987-06-11.

Classification & Regulation

This clearance is catalogued under FDA product code CFJ and 21 CFR 862.1440, within the Clinical Chemistry review panel as a Class II device.