510(k) K932653 ยท LGH Instrument, Cast Removal, Ac-Powered
SWISSTEK 2000(TM) CAST REMOVAL SYSTEM
| Applicant | Carapace, Inc., Broken Arrow OK, US |
| Decision | Substantially Equivalent, Jan 28, 1994 |
| Received | Jun 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932653
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.