510(k) K082280 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
SURESIGNS VS2 VITAL SIGNS MONITOR, SURESIGNS VM1 PATIENT MONITOR, SURESIGNS VS3 CITAL SIGNS MONITOR
| Applicant | Philips Medical Systems North America Co., Bothell WA, US |
| Decision | Substantially Equivalent, Oct 8, 2008 |
| Received | Aug 11, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082280
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.