510(k) K960468 ยท BTM Ventilator, Emergency, Manual (Resuscitator)
DMR/CO2 COMBO KTI
| Applicant | Nellcor Puritan Bennett, Inc., Pleasanton CA, US |
| Decision | Unknown, Apr 26, 1996 |
| Received | Feb 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960468
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.