Class Class U
TRAUMAGEL® (K240713)
Description
TRAUMAGEL® by Cresilon, Inc., an FDA 510(k) cleared unknown device.
Regulatory Information
Device ClassClass Class U
510(k) NumberK240713
Clearance Date2024-08-14
Clearance TypeTraditional
Product CodeQSY
FDA Database
View on FDA DatabasePredicate lineage for K240713
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. TRAUMAGEL® (K240713) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K113560 | CELOX GAUZE PRO | Medtrade Products , Ltd. | 2012 |
Trace the full predicate network for K240713
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.