meddevicedb.com FDA Device Reference

BIOTROL LACTATE DEHYDROGENASE (L-P)

K905683 Class II Traditional
Decision Date
1991-03-11
Sponsor / Applicant
Biotrol, USA, Inc.

Technical Specification

510(k) Submission ID K905683
Product Code CFJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1440
Decision Date 1991-03-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOTROL LACTATE DEHYDROGENASE (L-P) received FDA 510(k) clearance under submission number K905683, sponsored by Biotrol, USA, 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 1991-03-11.

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.