PIPETTER-DILUTER (MODEL 273)— 510(k) K761019

Name: FDA 510(k) clearance K761019
Creator: U.S. Food and Drug Administration
Published: 1976-11-16

Substantially Equivalent

Beckman Instruments, Inc.

FDA 510(k) clearance K761019 for PIPETTER-DILUTER (MODEL 273), Substantially Equivalent on 1976-11-16. Applicant: Beckman Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Beckman Instruments, Inc.
Product code: Code JRW
Device class: Class 1
Regulation: 21 CFR 866.3065
Advisory panel: Microbiology
Date received: 1976-11-11
Decision date: 1976-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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