Porous Media Corp.
Porous Media Corp. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Aug 8, 2006.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K062091 | POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION | Aug 8, 2006 |
| K061426 | OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47 | Jun 5, 2006 |
| K990276 | POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER | Oct 1, 1999 |
| K982385 | POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER | Feb 1, 1999 |
| K982127 | POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTER | Jun 23, 1998 |
| K965020 | POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER | Mar 14, 1997 |
| K964979 | POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER | Mar 11, 1997 |
| K952428 | POROUS MEDIA DBF23-R REUSABLE RESPIRATORY FILTER | Jul 7, 1995 |
| K934132 | POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER | Oct 4, 1994 |