510(k) K902261 ยท BTM Ventilator, Emergency, Manual (Resuscitator)
AMBU SPUR (SINGLE PATIENT USE RESUSCITATOR) INFANT
| Applicant | Ambu, Inc., Hanover MD, US |
| Decision | Substantially Equivalent, Jul 16, 1990 |
| Received | May 21, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902261
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.