ONPX-INDOL MEDIUM MICROTUBES— 510(k) K812466

Name: FDA 510(k) clearance K812466
Creator: U.S. Food and Drug Administration
Published: 1981-09-14

Substantially Equivalent

Carr Microbiologicals

FDA 510(k) clearance K812466 for ONPX-INDOL MEDIUM MICROTUBES, Substantially Equivalent on 1981-09-14. Applicant: Carr Microbiologicals. Device class: 1.

Clearance details

Applicant: Carr Microbiologicals
Product code: Code JSE
Device class: Class 1
Regulation: 21 CFR 866.2320
Advisory panel: Microbiology
Date received: 1981-08-31
Decision date: 1981-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K812470 — HIPP MICROTUBE1981-09-14

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