510(k) K172610 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
THUNDERBEAT 5 mm, 20 cm, Front-actuated Grip Type S, THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip Type S, THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S
| Applicant | Olympus Medical Systems Corp., Hachioji-Shi, JP |
| Decision | Substantially Equivalent, Apr 17, 2018 |
| Received | Aug 31, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172610
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 17, 2026 | Olympus Corporation of the Americas Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S Open, Classified |
LFL | None listed |
| Feb 17, 2026 | Olympus Corporation of the Americas Olympus Thunderbeat, 5 mm, 35 cm, Front-Actuated Grip Type S Open, Classified |
LFL | None listed |
| Feb 17, 2026 | Olympus Corporation of the Americas Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S Open, Classified |
LFL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.