K242828
- 510(k) number
- K242828
- 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
- 2024-10-18
- Date received
- 2024-09-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K242828.pdf
Official FDA record: K242828
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.