510(k) K132405 ยท DQD Stethoscope, Electronic
PPA/BT-RB STETHOSCOPE
| Applicant | Rnk Products, Inc., Melbourne FL, US |
| Decision | Substantially Equivalent, Oct 11, 2013 |
| Received | Aug 2, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132405
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.