Medical Device Manufacturer · US , Fort Lauderdale , FL

Digitimer , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2005

Total

Cleared

Denied

Digitimer , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.

Historical record: 2 cleared submissions from 2005 to 2018. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Digitimer , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Digitimer , Ltd.

2 devices

1-2 of 2