510(k) K873723 ยท LGH Instrument, Cast Removal, Ac-Powered
PLASTER VACUUM, 230V MODEL NO. 4183-161
| Applicant | Martin Medical, Desoto KS, US |
| Decision | Substantially Equivalent, Dec 10, 1987 |
| Received | Sep 15, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873723
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.