Medical Device Manufacturer · US , Alpharetta , GA

Sanuwave, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2017

1

Total

0

Cleared

1

Denied

Sanuwave, Inc. has 0 FDA 510(k) cleared medical devices. Based in Alpharetta, US.

Active since 2017. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Sanuwave, Inc.

1 devices

1-1 of 1

Not Cleared Dec 28, 2017

dermaPACE System

DEN160037 · PZL

General & Plastic Surgery · 521d