K231325
- 510(k) number
- K231325
- Device name
- Corplex P / Theracor P / Allacor P
- Applicant
- Stimlabs, LLC GA · US
- Product code
- KGN — Wound Dressing With Animal-Derived Material(S)
- Decision date
- 2024-02-02
- Date received
- 2023-05-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K231325.pdf
Official FDA record: K231325
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.