510(k) K113304 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
BLADDER SCANNER
| Applicant | MEDA Co., Ltd., Potomac MD, US |
| Decision | Substantially Equivalent, Mar 23, 2012 |
| Received | Nov 8, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113304
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.