BECKMAN B-4 TEB BUFFER KIT— 510(k) K791290

Name: FDA 510(k) clearance K791290
Creator: U.S. Food and Drug Administration
Published: 1979-08-03

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K791290 for BECKMAN B-4 TEB BUFFER KIT, Substantially Equivalent on 1979-08-03. Applicant: Beckman Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code JBD
Device class: Class 2
Regulation: 21 CFR 864.7440
Advisory panel: Hematology
Date received: 1979-07-10
Decision date: 1979-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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