CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY— 510(k) K914510

Name: FDA 510(k) clearance K914510
Creator: U.S. Food and Drug Administration
Published: 1991-11-19

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K914510 for CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY, Substantially Equivalent on 1991-11-19. Applicant: Beckman Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code JFN
Device class: Class 2
Regulation: 21 CFR 862.1145
Advisory panel: Clinical Chemistry
Date received: 1991-10-09
Decision date: 1991-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

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