510(k) K013273 ยท DQA Oximeter
FUKUDA DENSHI MODEL HG-500, PULSE OXIMETER MODULE
| Applicant | Fukuda Denshi USA, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Dec 20, 2001 |
| Received | Oct 1, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013273
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.