Medical Device Manufacturer · SE , Jarfalla

Perimed AB - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2001

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Perimed AB Cardiovascular ✕

3 devices

1-3 of 3

Cleared May 05, 2016

Cardiovascular · 213d

Cleared Jul 03, 2012

Cardiovascular · 102d

Cleared Nov 06, 2001

PF 5050 PRESSURE UNIT, MODEL PF 5050

Cardiovascular · 141d