CULTURE AND SENSITIVITY KIT— 510(k) K791413

Substantially Equivalent

Biomedia, Inc.

FDA 510(k) clearance K791413 for CULTURE AND SENSITIVITY KIT, Substantially Equivalent on 1979-10-17. Applicant: Biomedia, Inc.. Device class: 2.

Clearance details

Applicant: Biomedia, Inc.
Product code: Code JTZ
Device class: Class 2
Regulation: 21 CFR 866.1700
Advisory panel: Microbiology
Date received: 1979-07-30
Decision date: 1979-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K821108 — BI PLATE-XLD/HEKTOEN #300121982-05-13
K811471 — MUELLER HINTON AGAR1981-06-18

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