510(k) K023793 ยท BTM Ventilator, Emergency, Manual (Resuscitator)
1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR
| Applicant | Portex, Inc., Keene NH, US |
| Decision | Substantially Equivalent, Feb 11, 2003 |
| Received | Nov 13, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023793
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.