Class Class U
Spectricept Skin and Wound Cleanser (K243875)
Description
Spectricept Skin and Wound Cleanser by Spectrum Antimicrobials, Inc., an FDA 510(k) cleared unknown device.
Regulatory Information
Device ClassClass Class U
510(k) NumberK243875
Clearance Date2025-04-21
Clearance TypeTraditional
Product CodeFRO
FDA Database
View on FDA DatabasePredicate lineage for K243875
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. Spectricept Skin and Wound Cleanser (K243875) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K213514 | Spectricept Skin and Wound Cleanser | Spectrum Antimicrobials, Inc. (Subs... | 2023 |
Trace the full predicate network for K243875
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.