510(k) K842900 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
PHILIPS SDR 1200
| Applicant | Philips Medical Systems, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Dec 13, 1984 |
| Received | Jul 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842900
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.