meddevicedb.com FDA Device Reference

LACTIC DEHYDROGENASE REAGENT SET

K831415 Class II Traditional
Decision Date
1983-06-16
Sponsor / Applicant
Sterling Biochemical, Inc.

Technical Specification

510(k) Submission ID K831415
Product Code CFJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1440
Decision Date 1983-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LACTIC DEHYDROGENASE REAGENT SET received FDA 510(k) clearance under submission number K831415, sponsored by Sterling Biochemical, 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 1983-06-16.

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.