510(k) K900162 ยท HDR Cap, Cervical
DGH A-SAN PROBE HOLDER
| Applicant | Jedmed Instrument Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Feb 16, 1990 |
| Received | Jan 12, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900162
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.