K242758
- 510(k) number
- K242758
- Device name
- Atrauman® Ag
- Applicant
- Hartmann USA, Inc. SC · US
- Product code
- FRO — Dressing, Wound, Drug
- Decision date
- 2024-12-09
- Date received
- 2024-09-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242758.pdf
Official FDA record: K242758
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.