Medical Device Manufacturer · DE , Berlin

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

1 submissions · 1 cleared · Since 2017

Recent clearances: TONOPORT VI

1
Total
1
Cleared
0
Denied

FDA 510(k) Regulatory Record - Par Medizintechnik GmbH & Co. KG Cardiovascular ✕

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