Medical Device Manufacturer · US , Littleton , CO

Livetec GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2013

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Livetec GmbH Physical Medicine ✕

3 devices

1-3 of 3

Cleared Jan 13, 2015

3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200

Physical Medicine · 112d

Cleared Nov 07, 2014

Power Twin21-50/Power Twin21-100

Physical Medicine · 87d

Cleared Oct 10, 2013

3B LASER NEEDLE

Physical Medicine · 114d