510(k) K960473 ยท GET Motor, Surgical Instrument, Pneumatic Powered
AESCULAP POWER SYSTEM HANDPIECE
| Applicant | Aesculap, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent, Mar 7, 1996 |
| Received | Feb 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960473
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.