Medical Device Manufacturer · US , Baltimore , MD

Elekta Inc. D/B/A Nucletron Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

Total

Cleared

Denied

Elekta Inc. D/B/A Nucletron Corporation has 1 FDA 510(k) cleared medical devices. Based in Baltimore, US.

Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Elekta Inc. D/B/A Nucletron Corporation Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Elekta Inc. D/B/A Nucletron Corporation

1 devices

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