510(k) K910226 ยท HAO Instrument, Surgical, Non-Powered
DURAL DISSECTORS
| Applicant | Acra Cut, Inc., Acton MA, US |
| Decision | Substantially Equivalent, Feb 12, 1991 |
| Received | Jan 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910226
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.