EMB/MUELLER-HINTON AGAR— 510(k) K790369

Substantially Equivalent

Biomedia, Inc.

FDA 510(k) clearance K790369 for EMB/MUELLER-HINTON AGAR, Substantially Equivalent on 1979-04-23. 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: 1979-02-22
Decision date: 1979-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JTZ

K132491 — MUELLER HINTON AGAR2014-06-30
K963036 — MUELLER HINTON II BROTH (CATION-ADJUSTED) WITH LYSED HORSE BLOOD1996-10-07
K960420 — MUELLER HINTON AGAR WITH 5% SHEEP BLOOD1996-04-04
K960313 — MUELLER HINTON AGAR WITH 2% NACI1996-03-25
K945911 — CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGARS1995-04-04

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
K811471 — MUELLER HINTON AGAR1981-06-18

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