Medical Device Manufacturer · SE , Sloane

Pd International AB

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Pd International AB — FDA 510(k) Submissions

Pd International AB has submitted 1 FDA 510(k) premarket notifications since 1994, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Probe, Periodontic . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

PROBE TIP/PERI PROBE/PERI PROBE COMP.

K936221 · EIX Probe, Periodontic · Dental

Aug 1994 217d

Pd International AB

Pd International AB — FDA 510(k) Submissions

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