Medical Device Manufacturer · US , Fairfax , VA

Oldelft Corp. of America - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1989

Total

Cleared

Denied

Oldelft Corp. of America has 9 FDA 510(k) cleared medical devices. Based in Fairfax, US.

Historical record: 9 cleared submissions from 1989 to 1998. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Oldelft Corp. of America Filter by specialty or product code using the sidebar.

Oldelft Corp. of America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Oldelft Corp. of America

9 devices

1-9 of 9

SIMULIX-MC CT EXTENSION

K932848 · JAK

Radiology · 285d

Cleared Jan 15, 1993

THERAPAX DXT 300 SERIES 3

K923584 · JAD

Radiology · 179d

Cleared Jun 05, 1992

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Oldelft Corp. of America - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Oldelft Corp. of America

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