510(k) K882285 ยท BTM Ventilator, Emergency, Manual (Resuscitator)
NONREBREATHING CIRCUIT
| Applicant | Dryden Corp., Indianapolis IN, US |
| Decision | Substantially Equivalent, Aug 16, 1988 |
| Received | Jun 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882285
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.