PROTEOSE NO. 3 AGAR— 510(k) K881552

Name: FDA 510(k) clearance K881552
Creator: U.S. Food and Drug Administration
Published: 1988-04-18

Substantially Equivalent

Acumedia Manufacturers, Inc.

FDA 510(k) clearance K881552 for PROTEOSE NO. 3 AGAR, Substantially Equivalent on 1988-04-18. Applicant: Acumedia Manufacturers, Inc.. Device class: 2.

Clearance details

Applicant: Acumedia Manufacturers, Inc.
Product code: Code JTY
Device class: Class 2
Regulation: 21 CFR 866.2410
Advisory panel: Microbiology
Date received: 1988-04-08
Decision date: 1988-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baltimore, MD, US

Download summary PDF View on FDA.gov ↗

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