INDOLE NITRATE MEDIUM— 510(k) K832568

Name: FDA 510(k) clearance K832568
Creator: U.S. Food and Drug Administration
Published: 1983-09-12

Substantially Equivalent

Acumedia Manufacturers, Inc.

FDA 510(k) clearance K832568 for INDOLE NITRATE MEDIUM, Substantially Equivalent on 1983-09-12. Applicant: Acumedia Manufacturers, Inc.. Device class: 1.

Clearance details

Applicant: Acumedia Manufacturers, Inc.
Product code: Code JSE
Device class: Class 1
Regulation: 21 CFR 866.2320
Advisory panel: Microbiology
Date received: 1983-08-02
Decision date: 1983-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.