meddevicedb.com FDA Device Reference

LIPASE REAGENT SET

K831874 Class I Traditional
Decision Date
1983-08-12
Sponsor / Applicant
Sterling Biochemical, Inc.

Technical Specification

510(k) Submission ID K831874
Product Code JGX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1705
Decision Date 1983-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIPASE REAGENT SET received FDA 510(k) clearance under submission number K831874, 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 1983-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code JGX and 21 CFR 862.1705, within the Clinical Chemistry review panel as a Class I device.