510(k) K871932 ยท LNK Laser For Gastro-Urology Use
MODEL 5050 SURGILASER FOR UROLOGY USE
| Applicant | Lasermatic, Inc., Dallas TX, US |
| Decision | Substantially Equivalent, Mar 25, 1988 |
| Received | May 19, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871932
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.