BECKMAN ALPHA-1-MICROGLOBULIN (A1M) REAGENT— 510(k) K933078

Name: FDA 510(k) clearance K933078
Creator: U.S. Food and Drug Administration
Published: 1994-01-11

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K933078 for BECKMAN ALPHA-1-MICROGLOBULIN (A1M) REAGENT, Substantially Equivalent on 1994-01-11. Applicant: Beckman Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code MGA
Device class: Class 1
Regulation: 21 CFR 866.5400
Advisory panel: Immunology
Date received: 1993-06-23
Decision date: 1994-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

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