510(k) K892123 ยท CAE Airway, Oropharyngeal, Anesthesiology
GOETTINGER EMERGENCY RESUSCITATION TUBE
| Applicant | Plastic Parts Corp., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Jul 14, 1989 |
| Received | Apr 3, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892123
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.