510(k) K014025 ยท DQA Oximeter
HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER
| Applicant | Hommed, LLC, Houston TX, US |
| Decision | Substantially Equivalent, Apr 9, 2002 |
| Received | Dec 6, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014025
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.