510(k) K001265 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
WELCH ALLYN INSTRUMENT INTERFACE MODULE
| Applicant | Welch Allyn, Inc., Skaneateles Falls NY, US |
| Decision | Substantially Equivalent, Jul 13, 2000 |
| Received | Apr 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001265
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.