Medical Device Manufacturer · US , St. Paul , MN

Porous Media Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1994

9

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Porous Media Corp. Anesthesiology ✕

1 devices

1-1 of 1

Cleared Aug 08, 2006

POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION

Anesthesiology · 15d