Medical Device Manufacturer · US , Milwaukee , WI

Instrumentarium Imaging, Inc. - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 1989

Total

Cleared

Denied

Instrumentarium Imaging, Inc. has 24 FDA 510(k) cleared radiology devices. Based in Milwaukee, US.

Historical record: 24 cleared submissions from 1989 to 2000.

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

Instrumentarium Imaging, 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 - Instrumentarium Imaging, Inc.

24 devices

1-12 of 24

Cleared Nov 29, 2000

DELTA 32 AND DELTA 32 TACT

DIAMOND (MAMMOGRAPHIC X-RAY SYSTEM)

ORTHOPANTOMOGRAPH OP100 AND ORTHOCEPH OC100

INSTRUMENTARIUM MEGA4 HT

K925987 · LNH

Radiology · 175d

Cleared May 17, 1993

INSTRUMENTARIUM MEGA4 HT

K924921 · LNH

Radiology · 234d

Cleared May 03, 1993

INSTRUMENTARIUM MEGA4 HT

K923581 · LNH

Radiology · 287d

Cleared May 03, 1993

INSTRUMENTARIUM MEGA4 HT

K924472 · LNH

Radiology · 243d

Cleared Oct 06, 1992

INSTRUMENTARIUM MEGA4 HT

K923352 · LNH

Radiology · 90d

Cleared Sep 22, 1992

INSTRUMENTARIUM MEGA4 HT

K923022 · LNH

Radiology · 91d

Instrumentarium Imaging, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Instrumentarium Imaging, Inc.

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