510(k) K001708 ยท DQA Oximeter
PROFOX SOFTWARE, MODEL 920M-41
| Applicant | Respironics Georgia, Inc., Marietta GA, US |
| Decision | Substantially Equivalent, Mar 1, 2001 |
| Received | Jun 5, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001708
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.