MODIFIED NEW YORK MEDIUM— 510(k) K831359

Name: FDA 510(k) clearance K831359
Creator: U.S. Food and Drug Administration
Published: 1983-05-18

Substantially Equivalent

Gibco Laboratories Life Technologies, Inc.

FDA 510(k) clearance K831359 for MODIFIED NEW YORK MEDIUM, Substantially Equivalent on 1983-05-18. Applicant: Gibco Laboratories Life Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Gibco Laboratories Life Technologies, Inc.
Product code: Code JTY
Device class: Class 2
Regulation: 21 CFR 866.2410
Advisory panel: Microbiology
Date received: 1983-04-26
Decision date: 1983-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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