Medical Device Manufacturer · US , Columbia , MD

Nucletron Corp. - FDA 510(k) Cleared Devices

27 submissions · 27 cleared · Since 1995

Total

Cleared

Denied

Nucletron Corp. has 27 FDA 510(k) cleared radiology devices. Based in Columbia, US.

Historical record: 27 cleared submissions from 1995 to 2009.

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 Corp.

27 devices

1-12 of 27

Cleared Oct 08, 2009

MICROSELECTRON HDR V2, MODEL 105.999

K092804 · JAQ

Radiology · 27d

Cleared Jun 29, 2009

LUMENCATH APPLICATOR SET, MODELS 189. 795, 189.796, 189.797, 189.798,...

K091598 · JAQ

Radiology · 26d

Cleared Sep 14, 2007

INTEGRATED BRACHYTHERAPY UNIT - DIGITAL

K072445 · KPQ

Radiology · 15d

Cleared Mar 24, 2005

INTRACAVITARY MOULD APPLICATOR SET, MODEL 189.001

SWIFT 2.0, MODEL 132.001

MICROSELECTRON HDR- GENIE AFTERLOADING SYSTEM, MODEL 105.989 FOR 115VOLT...

K021286 · JAQ

Radiology · 30d

Cleared Mar 13, 2002

IMPLANT GUIDANCE SYSTEM APPLICATOR SET

K020015 · JAQ

Radiology · 69d

Cleared Oct 17, 2001

SEED SELECTRON MODEL V. 1.0

K010032 · JAQ

Radiology · 287d

Cleared Sep 19, 2001

OLDELFT THORASCAN MODEL NUMBER 180T

K012165 · KPR

Radiology · 70d

Nucletron Corp. - FDA 510(k) Cleared Devices

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