510(k) K052619 ยท DQA Oximeter
THE FINGER GUARD
| Applicant | T F & G Products, Oroville CA, US |
| Decision | Substantially Equivalent, Jan 6, 2006 |
| Received | Sep 23, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052619
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.