Ogenix Corporation
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| EPIFLO; Transdermal continuous oxygen therapy device; single use; disposable medical devic recall (Z-1477-2012) | Ogenix Corporation | 2012-04-30 |
| Clinical Users Guide (CUG) accompanying the EpiFLO SD, Part #01-100-1000000. The EpiFLO is recall (Z-1526-06) | Ogenix Corporation | 2006-09-28 |
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Every clearance here is in the API, with alerts when new ones post.