Porous Media Corp. is one of 18344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Porous Media Corp. - FDA 510(k) Cleared Devices
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
9
Total
9
Cleared
0
Denied
Porous Media Corp. has 9 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 9 cleared submissions from 1994 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Porous Media Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Porous Media Corp.
9 devices
Cleared
Aug 08, 2006
POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION
Anesthesiology
15d
Cleared
Jun 05, 2006
OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47
General Hospital
13d
Cleared
Oct 01, 1999
POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER
Cardiovascular
246d
Cleared
Feb 01, 1999
POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER
Cardiovascular
207d
Cleared
Jun 23, 1998
POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTER
General Hospital
6d
Cleared
Mar 14, 1997
POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER
General Hospital
88d
Cleared
Mar 11, 1997
POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER
General Hospital
89d
Cleared
Jul 07, 1995
POROUS MEDIA DBF23-R REUSABLE RESPIRATORY FILTER
General Hospital
44d
Cleared
Oct 04, 1994
POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER
General Hospital
405d