K233026
- 510(k) number
- K233026
- Device name
- Midmark Smart M9® Sterilizer, Midmark Smart M11® Sterilizer
- Applicant
- Midmark Corporation OH · US
- Product code
- FLE — Sterilizer, Steam
- Decision date
- 2024-04-04
- Date received
- 2023-09-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K233026.pdf
Official FDA record: K233026
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.