510(k) K952292 ยท BZD Ventilator, Non-Continuous (Respirator)
PURITAN-BENNETT COMPANION NASAL CPAP SYSTEM
| Applicant | Puritan Bennett Corp., Lenexa KS, US |
| Decision | Substantially Equivalent, Nov 13, 1995 |
| Received | May 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952292
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.