Class Class II
SonoBlock; SonoBlock II (K241954)
Description
SonoBlock; SonoBlock II by PAJUNK GmbH Medizintechnologie, an FDA 510(k) cleared anesthesiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241954
Clearance Date2024-09-11
Clearance TypeTraditional
Product CodeBSP
Regulation Number868.5150
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241954
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. SonoBlock; SonoBlock II (K241954) cites 1 predicate device and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K111374 | SONO-SERIES CORNERSTONE TECHNIQUE | PAJUNK GmbH Medizintechnologie | 2011 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K243682 | SonoPlex STIM; SonoPlex II | PAJUNK GmbH Medizintechnologie | 2025 |
Trace the full predicate network for K241954
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.