Class Class II
ClearHemograsper (K242857)
Description
ClearHemograsper by Finemedix Co., Ltd., an FDA 510(k) cleared gastroenterology, urology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242857
Clearance Date2025-05-21
Clearance TypeTraditional
Product CodeKGE
Regulation Number876.4300
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242857
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. ClearHemograsper (K242857) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K062517 | ELECTROSURGICAL HEMOSTATIC FORCEPS SERIES | Olympus Medical Systems Corporation | 2006 |
Trace the full predicate network for K242857
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.