510(k) K893380 ยท LGH Instrument, Cast Removal, Ac-Powered
QCR SYSTEM I AND QCR SYSTEM II
| Applicant | Bremer Mfg. & Tool Co., Inc., Winter Park FL, US |
| Decision | Substantially Equivalent, Nov 16, 1989 |
| Received | May 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893380
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.