Medical Device Manufacturer · US , Washington , DC

Kundt + Co. AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1984

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kundt + Co. AG General Hospital ✕

1 devices

1-1 of 1

Cleared Oct 09, 1984

MED. SUPPORT STOCKING-VENOFIT LASTOFLEX

General Hospital · 89d