Medical Device Manufacturer · US , Sunnyvale , CA

Denoptix, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1996

Total

Cleared

Denied

Denoptix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Denoptix, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Denoptix, Inc.

1 devices

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