510(k) K924752 ยท DQA Oximeter
FREEDOM OXIMETER/EEG DIGITAL INTERFACE
| Applicant | Pro-Tech, Inc., Woodinville WA, US |
| Decision | Substantially Equivalent, Sep 10, 1993 |
| Received | Sep 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924752
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.