K233578
- 510(k) number
- K233578
- Device name
- BAHADIR STERILIZATION CONTAINERS
- Applicant
- Bahadir USA, LLC NJ · US
- Product code
- KCT — Sterilization Wrap Containers, Trays, Cassettes & Ot
- Decision date
- 2024-03-22
- Date received
- 2023-11-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K233578.pdf
Official FDA record: K233578
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.