510(k) K871864 ยท DQA Oximeter
PB240 PATIENT MONITOR/PULSE OXIMETER
| Applicant | Puritan Bennett Corp., Overland Park KS, US |
| Decision | Substantially Equivalent, Jun 24, 1987 |
| Received | May 13, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871864
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.