510(k) K022453 ยท DSI Detector And Alarm, Arrhythmia
MODIFICATION TO ACUITY CENTRAL MONITORING SYSTEM
| Applicant | Welch Allyn Protocol, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, Aug 21, 2002 |
| Received | Jul 26, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022453
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 13, 2004 | Welch Allyn Protocol, Inc Welch Allyn Acuity Central Monitoring Station (With SunBlade Model 150,650 MHZ. Part # 700-0362-00 Terminated |
DSI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.