BECKMAN DIATRAC HEMOGLOBIN A ELECTROPHORESIS KIT— 510(k) K905709

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K905709 for BECKMAN DIATRAC HEMOGLOBIN A ELECTROPHORESIS KIT, Substantially Equivalent on 1991-09-23. Applicant: Beckman Instruments, Inc..

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code LCP
Advisory panel: Hematology
Date received: 1990-12-21
Decision date: 1991-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.