Class Class II
PADLOCK CLIP EFTR Kit (00713229) (K240274)
Description
PADLOCK CLIP EFTR Kit (00713229) by STERIS Corporation, an FDA 510(k) cleared gastroenterology, urology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK240274
Clearance Date2024-09-17
Clearance TypeTraditional
Product CodePKL
Regulation Number876.4400
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240274
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. PADLOCK CLIP EFTR Kit (00713229) (K240274) cites 1 predicate device and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K170867 | FTRD System Set | Ovesco Endoscopy AG | 2017 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K250842 | PADLOCK CLIP EFTR Kit (00713229) | STERIS Corporation | 2025 |
Trace the full predicate network for K240274
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.