510(k) K072285 ยท ITX Transducer, Ultrasonic, Diagnostic
ALOKA SSD-ALPHA 7 ULTRASOUND SYSTEM
| Applicant | Aloka Co., Ltd., Wallingford CT, US |
| Decision | Substantially Equivalent, Aug 30, 2007 |
| Received | Aug 16, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072285
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.