Medical Device Manufacturer · US , Rapid City , SD

Rapid City Regional Hospital, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1985

Total

Cleared

Denied

Rapid City Regional Hospital, Inc. has 10 FDA 510(k) cleared microbiology devices. Based in Rapid City, US.

Historical record: 10 cleared submissions from 1985 to 1985.

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

Rapid City Regional Hospital, 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 - Rapid City Regional Hospital, Inc.

10 devices

1-10 of 10

Cleared Mar 25, 1985

CULTURE MEDIA NONSELECTIVE & NONDIFFERENTIAL

AMIES TRANSPORT MEDIA

K850717 · JSM

Microbiology · 28d

Cleared Mar 22, 1985

DNASE TEST MEDIA, CHRISTENSEN'S UREA AGAR

K850719 · JSH

Microbiology · 28d

Cleared Mar 22, 1985

EOSIN METHYLENE BLUE AGAR, SS AGAR, XLD AGAR 6.5%

K850720 · JSI

Microbiology · 28d

Cleared Mar 22, 1985

KLIGER'S IRON AGAR, SIM MEDIA, MRVP MEDIUM, BILE E

SABOURAUD'S DEXTROSE AGAR, BORDET GENGOU AGAR, MYC

Rapid City Regional Hospital, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Rapid City Regional Hospital, Inc.

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