meddevicedb.com FDA Device Reference

ALANINE AMINOTRANSFERASE

K884936 Class I Traditional
Decision Date
1989-01-03
Sponsor / Applicant
Catachem, Inc.

Technical Specification

510(k) Submission ID K884936
Product Code CKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1030
Decision Date 1989-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALANINE AMINOTRANSFERASE received FDA 510(k) clearance under submission number K884936, sponsored by Catachem, 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 1989-01-03.

Classification & Regulation

This clearance is catalogued under FDA product code CKA and 21 CFR 862.1030, within the Clinical Chemistry review panel as a Class I device.