Medical Device Manufacturer · DE , Neumuenster

Transcoject GmbH & Co. KG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985
1
Total
1
Cleared
0
Denied

Transcoject GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Neumuenster, DE.

Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Transcoject GmbH & Co. KG Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Transcoject GmbH & Co. KG

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