510(k) K900660 ยท JAK System, X-Ray, Tomography, Computed
TOMOSCAN STEREOTAXIS SIMULATION SOFTWARE
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Mar 13, 1990 |
| Received | Feb 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900660
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.