510(k) K895861 ยท LGH Instrument, Cast Removal, Ac-Powered
DELTA-TECH(TM) CAST REMOVAL SYSTEM
| Applicant | Johnson & Johnson Professionals, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Oct 19, 1989 |
| Received | Oct 3, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895861
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.