510(k) K872389 ยท HXX Screwdriver
PRECISION SCREW DRIVER SET
| Applicant | Med-Tool, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Jul 15, 1987 |
| Received | Jun 19, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872389
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.