510(k) K033378 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
VITAL SIGNS MONITOR, PROPAQ LT
| Applicant | Welch Allyn Protocol, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, Mar 1, 2004 |
| Received | Oct 22, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033378
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 7, 2014 | Welch Allyn Protocol, Inc The Propaq LT Series monitors. Model numbers 802LTAN, 802LT0N, and 802LTRN.
These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for Terminated |
MWI | None listed |
| Nov 28, 2006 | Welch Allyn Protocol, Inc Propaq LT vital signs monitor, Model 802LTON Terminated |
MWI | None listed |
| Nov 28, 2006 | Welch Allyn Protocol, Inc Propaq LT vital signs monitor, Model 802LTRN Terminated |
MWI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.