K243930
- 510(k) number
- K243930
- Device name
- Sonopet iQ Ultrasonic Aspirator System (5500-050-000)
- Applicant
- Stryker Instruments MI · US
- Product code
- LFL — Instrument, Ultrasonic Surgical
- Decision date
- 2025-03-24
- Date received
- 2024-12-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K243930.pdf
Official FDA record: K243930
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.