MRSA SCREEN AGAR (MUELLER HINTON W/NACL & OXACIL.)— 510(k) K870649

Name: FDA 510(k) clearance K870649
Creator: U.S. Food and Drug Administration
Published: 1987-04-14

Substantially Equivalent

Hardy Media

FDA 510(k) clearance K870649 for MRSA SCREEN AGAR (MUELLER HINTON W/NACL & OXACIL.), Substantially Equivalent on 1987-04-14. Applicant: Hardy Media. Device class: 2.

Clearance details

Applicant: Hardy Media
Product code: Code JTZ
Device class: Class 2
Regulation: 21 CFR 866.1700
Advisory panel: Microbiology
Date received: 1987-02-13
Decision date: 1987-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Barbara, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JTZ

view all

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 Hardy Media

view all

K880116 — MRVP BROTH1988-03-31
K880119 — MOELLERS DECARBOXYLASE, ONITHINE1988-03-31
K880120 — MOELLERS DECARBOXYLASE, LYSINE1988-03-31
K880121 — MOELLERS DECARBOXYLASE, BASE1988-03-31
K880122 — MIDDLEBROOK 7H9 BROTH1988-03-31

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