K234132
- 510(k) number
- K234132
- Device name
- Medline Reusable Sterilization Wrappers
- Applicant
- Medline Industries, LP IL · US
- Product code
- FRG — Wrap, Sterilization
- Decision date
- 2024-09-17
- Date received
- 2023-12-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K234132.pdf
Official FDA record: K234132
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.