K252640
- 510(k) number
- K252640
- Device name
- VereSee Optical Veres Needle and Endoscopic Camera
- Applicant
- Freyja Healthcare, LLC MA · US
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2025-10-20
- Date received
- 2025-08-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252640.pdf
Official FDA record: K252640
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.