Medical Device Manufacturer · US , Mchenry , IL

Carr-Scarborough Microbiologicals, Inc. - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 1979

Total

Cleared

Denied

Carr-Scarborough Microbiologicals, Inc. has 24 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.

Historical record: 24 cleared submissions from 1979 to 1994.

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

Carr-Scarborough Microbiologicals, 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 - Carr-Scarborough Microbiologicals, Inc.

24 devices

1-24 of 24

Cleared Oct 04, 1994

BRAIN HEART INFUSION AGAR

K944554 · JSO

Microbiology · 18d

Cleared Aug 24, 1994

MUELLER HINTON AGAR W/OXACILLIN

M. CAT. BUTYRATE DISC

RAPID GLUTAMIC ACID DECARBOXYLASE (GDC) MICROTUBE

CSM CHROMOGENIC B-LACTAMASE DISC

K822930 · JTO

Microbiology · 28d

Cleared Sep 21, 1982

CSM BETA-LACTAMASE DISC

ACRIDINE ORANGE STAIN

K812212 · IDC

Microbiology · 27d

Cleared Sep 01, 1981

AURAMINE O MYCROBACTERIAL STAIN SET

K812274 · KJK

Microbiology · 19d

Cleared Aug 18, 1981

IDS RAPIDS NH SYSTEMS

K812048 · JSX

Microbiology · 29d

Cleared Aug 07, 1981

IDS BETA-LACTAMASE DISC

BETA LACTAMASE REAGENT DISK

K802566 · JTO

Microbiology · 14d

Cleared Oct 17, 1979

IMPROVED GRAM STAIN REAGENTS

K791711 · HYI

Microbiology · 50d

Carr-Scarborough Microbiologicals, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Carr-Scarborough Microbiologicals, Inc.

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