Medical Device Manufacturer · US , St. Paul , MN

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

9 submissions · 9 cleared · Since 1994

Recent clearances: POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION, OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47, POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER

View 9 510(k) Devices ↓

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

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 06, 2026