510(k) K092342 ยท NYV Gastrointestinal Motility System, Capsule
SMARTPILL GI MONITORING SYSTEM, VERSION 2.0
| Applicant | The Smartpill Corporation, Buffalo NY, US |
| Decision | Substantially Equivalent, Oct 30, 2009 |
| Received | Aug 4, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092342
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.