510(k) K881881 ยท BTM Ventilator, Emergency, Manual (Resuscitator)
OXYGENATION CATHETER
| Applicant | Ventech Healthcare Corp., Inc., Norcross GA, US |
| Decision | Substantially Equivalent, Feb 17, 1989 |
| Received | May 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881881
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.