510(k) K982623 ยท GCJ Laparoscope, General & Plastic Surgery
AESCULAP NEEDLESCOPIC INSTRUMENT SYSTEM
| Applicant | Aesculap, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent, Sep 30, 1998 |
| Received | Jul 28, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982623
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.