Medical Device Manufacturer · DE , Berlin

Par Medizintechnik GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

Par Medizintechnik GmbH has 1 FDA 510(k) cleared medical devices. Based in Berlin, DE.

Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Par Medizintechnik GmbH Filter by specialty or product code using the sidebar.

Par Medizintechnik GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Par Medizintechnik GmbH

1 devices

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