Medical Device Manufacturer · US , Walker , MI

Otisville Biotech, Inc. - FDA 510(k) Cleared Devices

98 submissions · 98 cleared · Since 1983

Total

Cleared

Denied

Otisville Biotech, Inc. has 98 FDA 510(k) cleared microbiology devices. Based in Walker, US.

Historical record: 98 cleared submissions from 1983 to 1986.

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

Otisville Biotech, Inc. 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 - Otisville Biotech, Inc.

98 devices

1-12 of 98

Cleared Jul 03, 1986

BIOTIS HAEMOPHILUS IDENTIFICATION QUAD

BIOTIS ACETAMIDE AGAR

K862389 · JSI

Microbiology · 9d

Cleared Jul 03, 1986

BIOTIS BORDET GENGOU AGAR

K862390 · KZI

Microbiology · 9d

Cleared Jul 03, 1986

BIOTIS DESOXYCHOLATE AGAR

K862391 · JSI

Microbiology · 9d

Cleared Jul 03, 1986

BIOTIS MOTILITY TEST MEDIUM

BIOTIS MITIS SALIVARIUS

K862394 · JSI

Microbiology · 9d

Cleared Jul 03, 1986

BIOTIS DECARBOXYLASE MEDIA, BASE

K862395 · JSH

Microbiology · 9d

Cleared Jul 03, 1986

BIOTIS DECARBOXYLASE MEDIA, ARGININE

K862396 · JSF

Microbiology · 9d

Cleared Jul 03, 1986

BIOTIS DECARBOXYLASE MEDIA, LYSINE

K862397 · JSF

Microbiology · 9d

Cleared Jul 03, 1986

BIOTIS DECARBOXYLASE MEDIA, ORNITHINE

K862398 · JSF

Microbiology · 9d

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Otisville Biotech, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Otisville Biotech, Inc.

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