510(k) K932307 ยท KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment
3M MAXI-DRIVER II DBATTERY POWERED SYSTEM
| Applicant | 3M Health Care, Ltd., St. Paul MN, US |
| Decision | Substantially Equivalent, Jan 7, 1994 |
| Received | May 11, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932307
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.