Porous Media Corp.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K062091 | POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION | BTT | 2006-08-08 | View |
| 510(k) | K061426 | OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47 | CAH | 2006-06-05 | View |
| 510(k) | K990276 | POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER | KRJ | 1999-10-01 | View |
| 510(k) | K982385 | POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER | KRJ | 1999-02-01 | View |
| 510(k) | K982127 | POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTER | CAH | 1998-06-23 | View |
| 510(k) | K965020 | POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER | CAH | 1997-03-14 | View |
| 510(k) | K964979 | POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER | CAH | 1997-03-11 | View |
| 510(k) | K952428 | POROUS MEDIA DBF23-R REUSABLE RESPIRATORY FILTER | CAH | 1995-07-07 | View |
| 510(k) | K934132 | POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER | CAH | 1994-10-04 | View |
No matching devices.
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