K232625
- 510(k) number
- K232625
- Device name
- Steriking® Pouch for Robotic Instruments
- Applicant
- Wipak OY FI
- Product code
- FRG — Wrap, Sterilization
- Decision date
- 2024-06-07
- Date received
- 2023-08-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K232625.pdf
Official FDA record: K232625
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.