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LDH (OPTIMIZED) REAGENT

K860029 Class II Traditional
Decision Date
1986-02-06
Sponsor / Applicant
Sigma Chemical Co.

Technical Specification

510(k) Submission ID K860029
Product Code CFJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1440
Decision Date 1986-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LDH (OPTIMIZED) REAGENT received FDA 510(k) clearance under submission number K860029, sponsored by Sigma Chemical Co.. 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 1986-02-06.

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.