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ASPARTATE TRANSAMINASE

K780039 Class II Traditional
Decision Date
1978-01-31
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K780039
Product Code CIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1100
Decision Date 1978-01-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASPARTATE TRANSAMINASE received FDA 510(k) clearance under submission number K780039, sponsored by Beckman Instruments, 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 1978-01-31.

Classification & Regulation

This clearance is catalogued under FDA product code CIT and 21 CFR 862.1100, within the Clinical Chemistry review panel as a Class II device.