510(k) K912265 ยท FED Endoscopic Access Overtube, Gastroenterology-Urology
MEDILASE SEMI-RIGID INSTROD SHEATH SERIES AE1000
| Applicant | Medical Laser, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 10, 1991 |
| Received | May 22, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912265
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.