LACTATE DEHYDROGENASE— 510(k) K780041

Name: FDA 510(k) clearance K780041
Creator: U.S. Food and Drug Administration
Published: 1978-02-01

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K780041 for LACTATE DEHYDROGENASE, Substantially Equivalent on 1978-02-01. Applicant: Beckman Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code CFJ
Device class: Class 2
Regulation: 21 CFR 862.1440
Advisory panel: Clinical Chemistry
Date received: 1978-01-09
Decision date: 1978-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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