Medical Device Manufacturer · US , Sunnyvale , CA

Aptus Endosystems - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2014

Recent clearances: APTUS HELI-FX ANCILLARY ENDOANCHOR CASSETTE

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aptus Endosystems Cardiovascular ✕

1 devices

1-1 of 1

Cleared May 16, 2014

APTUS HELI-FX ANCILLARY ENDOANCHOR CASSETTE

Cardiovascular · 23d