Medical Device Manufacturer · IT , Campli (Teramo)

Pentaferte S.P.A

2 submissions · 2 cleared · Since 2005

Total

Cleared

Denied

Pentaferte S.P.A — FDA 510(k) Submissions

Pentaferte S.P.A has submitted 2 FDA 510(k) premarket notifications since 2005, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Set, Administration, Intravascular, Set, Blood Transfusion . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

PENTATRASFU BLOOD TRANSFUSION SETS

K041496 · BRZ Set, Blood Transfusion · General Hospital

Jun 2005 391d

PENTADEFLUE IV SOLUTION ADMINISTRATION SETS

K041495 · FPA Set, Administration,... · General Hospital

Apr 2005 315d

Data Source

FDA 510(k) public files . 174,402 total devices indexed.

Pentaferte S.P.A

Pentaferte S.P.A — FDA 510(k) Submissions

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