Medical Device Manufacturer · US , Sacramento , CA

Central Media - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1987

Total

Cleared

Denied

Central Media has 14 FDA 510(k) cleared microbiology devices. Based in Sacramento, US.

Historical record: 14 cleared submissions from 1987 to 1987.

Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Central Media is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Central Media

14 devices

1-12 of 14

Cleared Nov 06, 1987

GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.

K873257 · JSG

Microbiology · 87d

Cleared Nov 06, 1987

STREPTOCOCCAL SELECTIVE DIFFEREN. & ENRICHED MEDIA

CORYNEBACTERIA ISOLATION MEDIA

ACTINOMYCETE DIFFERENTIAL MEDIA

K873270 · JSH

Microbiology · 85d

Cleared Oct 28, 1987

ENTERIC ISOLATION MEDIA

MAINTENANCE & CARBOHYDRATE FERMENTATION MEDIA

K873263 · JSH

Microbiology · 78d

Cleared Oct 28, 1987

MEDIA FOR DETECTION & VERIFICATION OF COLIFORMS

K873264 · JSI

Microbiology · 78d

Central Media - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Central Media

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