Medical Device Manufacturer · US , Mchenry , IL

Mds Laboratories, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1982

Total

Cleared

Denied

Mds Laboratories, Inc. has 21 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1982 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.

Mds Laboratories, 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 - Mds Laboratories, Inc.

21 devices

1-12 of 21

Cleared Mar 31, 1987

CARY BLAIR TRANSPORT MEDIUM

CLED AGAR WITH ANDRADES INDICATOR

K864239 · JSH

Microbiology · 154d

Cleared Mar 31, 1987

COLUMBIA BLOOD AGAR WITH 5% SHEEP BLOOD

GARNERELLA VAGINALIS IDENTIFICATION KIT

K864244 · JTO

Microbiology · 154d

Cleared Mar 31, 1987

MUELLER HINTON AGAR SMALL

K864245 · JTZ

Microbiology · 154d

Cleared Mar 31, 1987

MUELLER HINTON AGAR LARGE

K864246 · JTZ

Microbiology · 154d

Cleared Mar 31, 1987

MUELLER HINTON AGAR WITH 5% SHEEP BLOOD

K864247 · JTZ

Microbiology · 154d

Cleared Mar 31, 1987

MUELLER HINTON AGAR - SUPPLEMENTED

K864248 · JTZ

Microbiology · 154d

Mds Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Mds Laboratories, Inc.

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