510(k) K092307 ยท KPR System, X-Ray, Stationary
IMASIGHT 4600 DIGITAL RADIOGRAPHY SENSOR
| Applicant | Imasight, Inc., Gatineau, Quebec, CA |
| Decision | Substantially Equivalent, Aug 25, 2009 |
| Received | Jul 30, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092307
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.