LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT— 510(k) K872324

Name: FDA 510(k) clearance K872324
Creator: U.S. Food and Drug Administration
Published: 1987-08-19

Substantially Equivalent

Berthold Analytical Instruments, Inc.

FDA 510(k) clearance K872324 for LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT, Substantially Equivalent on 1987-08-19. Applicant: Berthold Analytical Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Berthold Analytical Instruments, Inc.
Product code: Code JJQ
Device class: Class 1
Regulation: 21 CFR 862.2300
Advisory panel: Clinical Chemistry
Date received: 1987-06-17
Decision date: 1987-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nashua, NH, US

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