TEST, MONO., DIFFERENTIAL SLIDE— 510(k) K760032

Name: FDA 510(k) clearance K760032
Creator: U.S. Food and Drug Administration
Published: 1976-08-03

Substantially Equivalent

Gamma Biologicals, Inc.

FDA 510(k) clearance K760032 for TEST, MONO., DIFFERENTIAL SLIDE, Substantially Equivalent on 1976-08-03. Applicant: Gamma Biologicals, Inc.. Device class: 1.

Clearance details

Applicant: Gamma Biologicals, Inc.
Product code: Code KIN
Device class: Class 1
Regulation: 21 CFR 864.3800
Advisory panel: Pathology
Date received: 1976-06-14
Decision date: 1976-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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