510(k) K013624 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
MODIFICATION TO AGILENT COMPONENT MONITORING SYSTEM (CMS), V24/V26 PATIENT MONITORS, BLOOD ANALYSIS PORTAL SYSTEM PLUG-I
| Applicant | Philips Medizin Systeme Boblingen GmbH, Andover MA, US |
| Decision | Substantially Equivalent, Dec 3, 2001 |
| Received | Nov 5, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013624
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.