Medical Device Manufacturer · US , St. Paul , MN

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

9 submissions · 9 cleared · Since 1994

Total

Cleared

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.

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

9 devices

1-9 of 9

Cleared Aug 08, 2006

POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION

K062091 · BTT

Anesthesiology · 15d

Cleared Jun 05, 2006

OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47

K061426 · CAH

General Hospital · 13d

Cleared Oct 01, 1999

POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER

K990276 · KRJ

Cardiovascular · 246d

Cleared Feb 01, 1999

POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER

K982385 · KRJ

Cardiovascular · 207d

Cleared Jun 23, 1998

POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTER

K982127 · CAH

General Hospital · 6d

Cleared Mar 14, 1997

POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER

K965020 · CAH

General Hospital · 88d

Cleared Mar 11, 1997

POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER

K964979 · CAH

General Hospital · 89d

Cleared Jul 07, 1995

POROUS MEDIA DBF23-R REUSABLE RESPIRATORY FILTER

K952428 · CAH

General Hospital · 44d

Cleared Oct 04, 1994

POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER

K934132 · CAH

General Hospital · 405d

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

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