510(k) K862149 ยท BXN Stimulator, Nerve, Battery-Powered
MODIFIED NEUROMUSCULAR TRANSMISSION MONITOR
| Applicant | Puritan Bennett Corp., Overland Park KS, US |
| Decision | Substantially Equivalent, Jun 19, 1986 |
| Received | Jun 4, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862149
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.