510(k) K043368 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
VITELCARE TURTLE, MODEL 400
| Applicant | Visual Telecommunications Network, Inc., Mclean VA, US |
| Decision | Substantially Equivalent, Feb 1, 2005 |
| Received | Dec 8, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K043368
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.