SYNCHRON CX SYSTEMS (LAP) REAGENT KIT— 510(k) K895850

Name: FDA 510(k) clearance K895850
Creator: U.S. Food and Drug Administration
Published: 1989-12-05

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K895850 for SYNCHRON CX SYSTEMS (LAP) REAGENT KIT, Substantially Equivalent on 1989-12-05. Applicant: Beckman Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code JGG
Device class: Class 1
Regulation: 21 CFR 862.1460
Advisory panel: Clinical Chemistry
Date received: 1989-10-03
Decision date: 1989-12-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

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