510(k) K131623 ยท JOP Transducer, Ultrasonic
SMARTDOP XT
| Applicant | Koven Technology, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Jan 17, 2014 |
| Received | Jun 4, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131623
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.