Medical Device Manufacturer · CH , Lausanne

Bracco Injeneering - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Bracco Injeneering has 1 FDA 510(k) cleared medical devices. Based in Lausanne, CH.

Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Bracco Injeneering Filter by specialty or product code using the sidebar.

Bracco Injeneering is one of 78 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Bracco Injeneering

1 devices

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