510(k) K873892 ยท LNK Laser For Gastro-Urology Use
SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE
| Applicant | Laserguide, Santa Barbara CA, US |
| Decision | Substantially Equivalent, Feb 2, 1988 |
| Received | Sep 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873892
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.