Medical Device Manufacturer · CA , Richmond Hill, Ontario

Wartner USA B.V. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Recent clearances: WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022)

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Wartner USA B.V. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Sep 10, 2003

WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022)

General & Plastic Surgery · 49d