510(k) K003965 ยท GEA Cannula, Surgical, General & Plastic Surgery
MRI SAFE INSTRUMENTS
| Applicant | Aesculap, Inc., Allentown PA, US |
| Decision | Substantially Equivalent, Mar 16, 2001 |
| Received | Dec 22, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003965
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.