Medical Device Manufacturer · US , Columbia , MD

Nucletron-Oldelft Corp. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1986

Total

Cleared

Denied

Nucletron-Oldelft Corp. has 11 FDA 510(k) cleared radiology devices. Based in Columbia, US.

Historical record: 11 cleared submissions from 1986 to 1996.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Nucletron-Oldelft Corp.

11 devices

1-11 of 11

Cleared Aug 13, 1996

MICROSELECTRON-HDR VERSION 2

MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT

K925956 · JAQ

Radiology · 360d

Cleared Mar 31, 1993

MODEL COLE TAB-2 TABLE W/MODEL COLE SFD-2 SPOTFILM

K926407 · KXJ

Radiology · 100d

Cleared Nov 27, 1992

PLATO RADIATION THERAPY PLANNING SYSTEM

K921991 · IYE

Radiology · 213d

Cleared Sep 25, 1992

PLATO BRACHYTHERAPHY TREATMENT PLANNING SYSTEM

K915622 · JAQ

Radiology · 284d

Cleared Jun 13, 1991

NUCLETRON PLANNING SYSTEM

MICROSELECTRON-HDR (HIGH DOSE RATE)

K864210 · JAQ

Radiology · 29d

Cleared May 21, 1986

MICROSELECTION INTERSTITIAL REMOTE AFTERLOAD SYS

K853912 · JAQ

Radiology · 243d

Cleared Jan 10, 1986

SELECTRON HDR REMOTE AFTERLOADER

K852842 · JAQ

Radiology · 189d

Nucletron-Oldelft Corp. - FDA 510(k) Cleared Devices

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