ClearanceBrief
Company ยท US

Porous Media Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 2006. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
CAHFilter, Bacterial, Breathing-Circuit6
BTTHumidifier, Respiratory Gas, (Direct Patient Interface)2
KRJFilter, Prebypass, Cardiopulmonary Bypass2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 8, 2006K062091POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION
Porous Media Corp.
BTT
Jun 5, 2006K061426OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47
Porous Media Corp.
CAH
Oct 1, 1999K990276POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER
Porous Media Corp.
KRJ
Feb 1, 1999K982385POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER
Porous Media Corp.
KRJ
Jun 23, 1998K982127POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTER
Porous Media Corp.
CAH
Mar 14, 1997K965020POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER
Porous Media Corp.
CAH
Mar 11, 1997K964979POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER
Porous Media Corp.
CAH
Jul 7, 1995K952428POROUS MEDIA DBF23-R REUSABLE RESPIRATORY FILTER
Porous Media Corp.
CAH
Oct 4, 1994K934132POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER
Porous Media Corp.
CAH

Latest recalls

DateFirm and productCodeLinked 510(k)
Jun 20, 2007Porous Media Corporation
HUMIDIFLOW Respiratory Gas Humidifier; Manufactured by: Porous Media Corporation 1350 Hammond Road St Paul, MN 55110, Part Number HMK-RM
Terminated
BTTK062091
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