510(k) K834384 ยท LGG Instrument, Cast Application/Removal, Manual
MODULAR EXTREMITY CASTING SUPPORT
| Applicant | Buckman Co., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 30, 1984 |
| Received | Dec 14, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834384
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.