Medical Device Manufacturer · US , Lake Oswego , OR

Biotronik AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005

Recent clearances: PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Biotronik AG Cardiovascular ✕

1 devices

1-1 of 1

Cleared Oct 28, 2005

PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER

Cardiovascular · 28d