Medical Device Manufacturer · DK , Taastrup

Auditdata A/S

1 submissions · 1 cleared · Since 2012
1
Total
1
Cleared
0
Denied

Auditdata A/S — FDA 510(k) Submissions

Auditdata A/S has submitted 1 FDA 510(k) premarket notifications since 2012, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Calibrator, Hearing Aid / Earphone And Analysis Systems . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
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All1 Ear, Nose, Throat 1