510(k) K983069 ยท OWB Interventional Fluoroscopic X-Ray System
PHILIPS DUO DIAGNOST
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Nov 2, 1998 |
| Received | Sep 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983069
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 16, 2012 | Philips Healthcare Inc. DuoDiagnost, model 707015, Universal RF system
Product Usage: is a mult-functional diagnostic X-Ray system intended for Fluorosopic, Radiographic, Angiographic, and Interventional applications. Terminated |
JAA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.