K231291
- 510(k) number
- K231291
- Device name
- Perforated Baskets
- Applicant
- Richard Wolf Medical Instruments Corporation IL · US
- Product code
- KCT — Sterilization Wrap Containers, Trays, Cassettes & Ot
- Decision date
- 2024-06-03
- Date received
- 2023-05-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K231291.pdf
Official FDA record: K231291
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.