Porous Media Corp.
Porous Media Corp. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2006.
Top product codes for Porous Media Corp.
Recent clearances by Porous Media Corp.
- K062091 — POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION
- K061426 — OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47
- K990276 — POROUS MEDIA DPB30 SERIES DISPOSABLE PRE-BYPASS FILTER
- K982385 — POROUS MEDIA DPB20 SERIES DISPOSABLE PRE-BYPASS FILTER
- K982127 — POROUS MEDIA DEF25 DISPOSABLE RESPIRATORY FILTER
- K965020 — POROUS MEDIA DBF23 REUSABLE RESPIRATORY FILTER
- K964979 — POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER
- K952428 — POROUS MEDIA DBF23-R REUSABLE RESPIRATORY FILTER
- K934132 — POROUS MEDIA DBF23 DISPOSABLE RESPIRATORY FILTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.