K233762
- 510(k) number
- K233762
- Device name
- SteroScope® Sterilization Technology System
- Applicant
- Ideate Medical, Inc. MO · US
- Product code
- MLR — Sterilizer, Chemical
- Decision date
- 2024-06-27
- Date received
- 2023-11-24
- 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: K233762.pdf
Official FDA record: K233762
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.