BLOOD-UREA-NITROGEN (BUN) ANALYZER 2— 510(k) K761061

Name: FDA 510(k) clearance K761061
Creator: U.S. Food and Drug Administration
Published: 1977-01-25

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K761061 for BLOOD-UREA-NITROGEN (BUN) ANALYZER 2, Substantially Equivalent on 1977-01-25. Applicant: Beckman Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code CDS
Device class: Class 2
Regulation: 21 CFR 862.1770
Advisory panel: Clinical Chemistry
Date received: 1976-11-18
Decision date: 1977-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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