510(k) K083229 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
E.S TECK ( ELECTRO SENSOR TECK)
| Applicant | Ld Technology, LLC, Miami FL, US |
| Decision | Substantially Equivalent, Feb 23, 2009 |
| Received | Nov 3, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083229
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.