Micro Media Laboratories
Micro Media Laboratories holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1985.
Top product codes for Micro Media Laboratories
Recent clearances by Micro Media Laboratories
- K853690 — COLUMBIZ BLOOD AGAR
- K853691 — TERGITOL 7 AGAR
- K851344 — OXIDATIVE FORMENTIVE MEDIUM
- K851343 — BROM CRESOL PURPLE STARCH
- K851345 — PURPLE BROTH
- K851346 — PHENYLALANINE AGAR
- K851347 — KANAMYCIN-VANCOMYCIN-LAKED BLOOD AGAR
- K851348 — COBA AGAR
- K850841 — MOD THAYER MARTIN MARTIN LEWIS
- K850842 — BRAIN HEART INFUSION BROTH
- K850843 — MUELLER HINTON CHOCOLATE AGAR
- K850844 — V AGAR
- K850845 — 0.85% SALINE
- K850846 — SALT BROTH
- K850847 — THIOGLYCOLATE MEDIUM W/VITAMIN KL & HEMIN
- K850848 — BRAIN HEART INFUSION AGAR
- K834020 — PEPTIC DIGEST AGAR
- K834005 — SELECTIVE STREPTOCOCCUS AGAR
- K834006 — BRUCELLA MEDIA
- K834010 — DERMATOPHYTE TEST MEDIUM
- K834008 — SABOURAUD DEXTROSE AGAR
- K834013 — SF BROTH
- K834001 — KLIGLER IRON AGAR
- K834002 — LYSINE IRON AGAR
- K834003 — MOTILITY INDOLE ORNITHINE-MEDIUM
- K834004 — MYCOBIOTIC AGAR
- K834007 — CYSTINE TRYPTIC MEDIUM
- K834009 — SIMMONS CITRATE AGAR
- K834012 — SIM MEDIUM
- K834014 — POTATO DEXTROSE AGAR
- K834015 — SELENITE BROTH
- K834016 — GN BROTH
- K834017 — CHOCOLATE AGAR W/CHEMICALLY DEFINED
- K834018 — CAMPY MEDIUM
- K834019 — BIGGY AGAR NICKERSON MEDIUM
- K811597 — UREA AGAR SLANT
- K811598 — DNASE AGAR MEDIA
- K811599 — EOSIN METHYLENE BLUE AGAR
- K811600 — BILE ESCULIN MEDIA
- K811601 — PHENYETHYL ALCOHOL AGAR
- K811602 — TRYPTIC SOY BROTH
- K811603 — SALMONELLA SHIGELLA AGAR
- K811604 — XYLOSE LYSINE DEOXYCHOLATE AGAR
- K811605 — HEKTOEN ENTERIC AGAR
- K811606 — FLUID THIOCLYCOLLATE MEDIUM
- K811607 — COLUMBIA AGAR CNA W/5% SHEEP BLOOD
- K811608 — MUELLER-HINTON
- K811609 — MANNITOL SALT AGAR
- K811610 — EOSIN METHYLENE BLUE AGAR (LEVINE)
- K811611 — MACCONKEY AGAR
- K811612 — TRYPTIC SOY AGAR
- K790497 — BACTERIOLOGICAL CULTURE MEDIA
Data sourced from openFDA. This site is unofficial and independent of the FDA.