Porous Media Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K062091POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATIONAugust 8, 2006
K061426OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47June 5, 2006
K990276POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTEROctober 1, 1999
K982385POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTERFebruary 1, 1999
K982127POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTERJune 23, 1998
K965020POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTERMarch 14, 1997
K964979POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTERMarch 11, 1997
K952428POROUS MEDIA DBF23-R REUSABLE RESPIRATORY FILTERJuly 7, 1995
K934132POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTEROctober 4, 1994