510(k) K081073 ยท OWB Interventional Fluoroscopic X-Ray System
HDR VISION, VISION HDR, HD R/F, UROMAT HD R/F
| Applicant | Pausch, LLC, Tenton Falls NJ, US |
| Decision | Substantially Equivalent, Dec 5, 2008 |
| Received | Apr 15, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081073
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.