Class Class U
coactiv+™ Antimicrobial Wound Gel (K241809)
Description
coactiv+™ Antimicrobial Wound Gel by Kane Biotech, Inc., an FDA 510(k) cleared unknown device.
Regulatory Information
Device ClassClass Class U
510(k) NumberK241809
Clearance Date2024-07-19
Clearance TypeSpecial
Product CodeFRO
FDA Database
View on FDA DatabasePredicate lineage for K241809
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. coactiv+™ Antimicrobial Wound Gel (K241809) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K223259 | coactiv+ Antimicrobial Wound Gel | Kane Biotech, Inc. | 2023 |
Trace the full predicate network for K241809
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.