Medical Device Manufacturer · US , Las Vegas , NV

Emergency Filtration Products, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998

Total

Cleared

Denied

Emergency Filtration Products, Inc. has 2 FDA 510(k) cleared medical devices. Based in Las Vegas, US.

Historical record: 2 cleared submissions from 1998 to 2002. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Emergency Filtration Products, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Emergency Filtration Products, Inc.

2 devices

1-2 of 2