K251893
- 510(k) number
- K251893
- Device name
- SKAN C PULSAR
- Applicant
- Skanray Technologies Limited IN
- Product code
- OWB — Interventional Fluoroscopic X-Ray System
- Decision date
- 2025-12-16
- Date received
- 2025-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 4.3 MB · U.S. public domain
Also available from FDA: K251893.pdf
Official FDA record: K251893
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.