510(k) K911098 ยท IXR Table, Radiographic, Tilting
PHILIPS URO DIAGNOST MRF
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Jul 3, 1991 |
| Received | Mar 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911098
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 30, 2019 | Philips North America, LLC UroDiagnost Eleva, system code 708033 Terminated |
IXR | None listed |
| Feb 28, 2019 | Philips North America, LLC Urodiagnost, Product No. 708033
Product Usage:
The Philips UroDiagnost MRF can be used to perform all urological and gynecological routine examinations including: Urograms with injection or infusio Terminated |
IXR | None listed |
| May 3, 2018 | Philips Medical Systems Nederlands 708033 URODiagnost
As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applica Terminated |
IXR | None listed |
| Jul 19, 2016 | Philips Electronics North America Corporation UroDiagnost; x-ray system. Product Code: 708033 Terminated |
IXR | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.