P-3 CLOSING INSTRUMENT
| Applicant | Lone Star Medical Products, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Feb 21, 1985 |
| Received | Jan 7, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850041
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.