510(k) K913135 ยท FSW Light, Surgical, Endoscopic
LM-300TWIN
| Applicant | Leisegang Medical, Inc., Boca Raton FL, US |
| Decision | Substantially Equivalent, Sep 18, 1991 |
| Received | Jul 16, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913135
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.