Medical Device Manufacturer · DE , Pullach

Gistlstrasse - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

Gistlstrasse has 1 FDA 510(k) cleared medical devices. Based in Pullach, DE.

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

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

Gistlstrasse 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 - Gistlstrasse

1 devices

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