MUELLER HINTON AGAR— 510(k) K811471

Substantially Equivalent

Biomedia, Inc.

FDA 510(k) clearance K811471 for MUELLER HINTON AGAR, Substantially Equivalent on 1981-06-18. 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: 1981-05-26
Decision date: 1981-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Biomedia, Inc.

K821300 — #2010 CAMPHYLOBACTER AGAR1982-06-02
K821301 — #50002 QUAD DIAGNOSTIC SYSTEM1982-06-01
K821302 — #50003 QUAD DIAGNOSTIC SYSTEM1982-06-01
K821108 — BI PLATE-XLD/HEKTOEN #300121982-05-13
K811472 — MUELLER HINTON AGAR, POURED INTO A PLATE1981-06-18

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