510(k) K984111 ยท KPR System, X-Ray, Stationary
FV-RF
| Applicant | Philips Medical Systems (Cleveland), Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Dec 11, 1998 |
| Received | Nov 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984111
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 18, 2016 | Philips Medical Systems (Cleveland) Inc FV-RF (Clinix RF Plus)
Product Usage:
A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis an Terminated |
KPR | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.