Medical Device Manufacturer · US , Salt Lake City , UT

Ge Dec Medical Systems - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1994

Recent clearances: SERIES 7700 MOBILE C-ARM, COMPACT 7700 MOBILE C-ARM, COMPACT 7700 PLUS MOBILE C-ARM, UROVIEW 2800, MINI 6800 DIGITAL MOBILE C-ARM

View 10 510(k) Devices ↓

Total

Cleared

Denied

Ge Dec Medical Systems has 10 FDA 510(k) cleared radiology devices. Based in Salt Lake City, US.

Historical record: 10 cleared submissions from 1994 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.

Ge Dec Medical Systems is one of 21482 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ge Dec Medical Systems

10 devices

1-10 of 10

Cleared Apr 11, 2000

SERIES 7700 MOBILE C-ARM, COMPACT 7700 MOBILE C-ARM, COMPACT 7700 PLUS MOBILE...

MINI 6800 DIGITAL MOBILE C-ARM

K992506 · OXO

Radiology · 23d

Cleared Feb 17, 1998

INTERVENTIONAL MOBILE DIGITAL IMAGING SYSTEM (HEREIN CALLED IMDIS)

K974355 · OWB

Radiology · 90d

Cleared Mar 11, 1997

SERIES 7600 MOBILE DIGITAL C-ARM

K970063 · OWB

Radiology · 63d

Cleared Dec 23, 1996

SERIES 9600 MOBILE DIGITAL IMAGING SYSTEM

SERIES 6600 DIGITAL MOBILE C-ARM

UROVIEW SYSTEMS TOMOGRAPHY OPTION SOFTWARE

K936136 · JAA

Radiology · 34d

Ge Dec Medical Systems - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Ge Dec Medical Systems

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