Class Class II
Boehringer Laboratories Liver Retractor (K243399)
Description
Boehringer Laboratories Liver Retractor by Boehringer Laboratories, LLC, an FDA 510(k) cleared gastroenterology, urology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243399
Clearance Date2025-07-02
Clearance TypeTraditional
Product CodeGCJ
Regulation Number876.1500
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243399
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. Boehringer Laboratories Liver Retractor (K243399) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K162445 | LiVac Retractor System | Livac Pty, Ltd. | 2016 |
Trace the full predicate network for K243399
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.