510(k) K953910 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile
PHILIPS BV 300 SERIES
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Oct 18, 1995 |
| Received | Aug 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953910
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 1, 2003 | Philips Medical Systems Philips BV300 Mobile X-Ray System Terminated |
IZL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.