510(k) K260544 ยท DQX Wire, Guide, Catheter
FMD Peripheral Guide Wire F-14 Flex 6; FMD Peripheral Guide Wire F-14 Tapered 40; FMD Peripheral Guide Wire F-18 Flex SP; FMD Peripheral Guide Wire F-18 DP 25; FMD Peripheral Guide Wire F-18 Tapered 40
| Applicant | FMD Co., Ltd., Shibuya-Ku, JP |
| Decision | Substantially Equivalent, Mar 20, 2026 |
| Received | Feb 18, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K260544
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.