510(k) K904859 ยท HRX Arthroscope
MOTOR DRIVEN EXTIRPATION INSTRUMENTS
| Applicant | Aesculap, Inc., Burlingame CA, US |
| Decision | Substantially Equivalent, Mar 15, 1991 |
| Received | Oct 29, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904859
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.