510(k) K101757 ยท ITX Transducer, Ultrasonic, Diagnostic
SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM, SONOSITE MAXX SERIES ULTRASOUND SYSTEM
| Applicant | Sonosite,Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Aug 12, 2010 |
| Received | Jun 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101757
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.