510(k) K033238 ยท IZL System, X-Ray, Mobile
MOBILETTE XP AND MOBILETT XPHYBRID
| Applicant | Siemens Medical Systems, Inc., Mavern PA, US |
| Decision | Substantially Equivalent, Nov 14, 2003 |
| Received | Oct 6, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033238
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 2, 2014 | Siemens Medical Solutions USA, Inc Siemens Mobilett XP Digital Mobile X-ray System
Product Usage: The Mobilett XP and Mobilett XP Hybrid are radiographic systems designed for use in wards, intensive care, and premature birth-wards, Terminated |
IZL | None listed |
| Dec 17, 2010 | Siemens Medical Solutions USA, Inc Mobilett XP Hybrid/Digital/CR
Intended use: mobile x-ray system Terminated |
IZL | None listed |
| Nov 1, 2010 | Siemens Medical Solutions USA, Inc Mobilett XP and Mobilett XP Hybrid, Mobile radiology device
System, x-ray, mobile Terminated |
IZL | None listed |
| Apr 19, 2007 | Siemens Medical Solutions USA, Inc Mobilett XP, mobile X-ray system, Model number 1818454 Terminated |
IZL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.