510(k) K062091 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
POROUS MEDIA HUMIDIFLOW HUMIDIFIER FOR UNIVERSAL HUMIDIFICATION
| Applicant | Porous Media Corp., St. Paul MN, US |
| Decision | Substantially Equivalent, Aug 8, 2006 |
| Received | Jul 24, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062091
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 20, 2007 | Porous Media Corporation HUMIDIFLOW Respiratory Gas Humidifier; Manufactured by: Porous Media Corporation 1350 Hammond Road St Paul, MN 55110, Part Number HMK-RM Terminated |
BTT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.