meddevicedb.com FDA Device Reference

ALANINE AMINOTRANSFERASE (ALT) TEST

K935180 Class I Traditional
Decision Date
1994-01-13
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K935180
Product Code CKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1030
Decision Date 1994-01-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALANINE AMINOTRANSFERASE (ALT) TEST received FDA 510(k) clearance under submission number K935180, sponsored by Em Diagnostic Systems, 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 1994-01-13.

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.