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.

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

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