510(k) K040995 ยท KPR System, X-Ray, Stationary
SYNERAD MULTI DIGITAL X-RAY SYSTEM, MODEL AN6150
| Applicant | Analogic Corp., Peabody MA, US |
| Decision | Substantially Equivalent, May 25, 2004 |
| Received | Apr 16, 2004 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K040995
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 24, 2005 | Analogic Corporation Analogic SyneRad Multi Digital Radiology System, Model AN6150 Terminated |
KPR | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.