K261139
- 510(k) number
- K261139
- Device name
- VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)
- Applicant
- Freyja Healthcare, LLC MA · US
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2026-08-13
- Date received
- 2026-04-07
- 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: K261139.pdf
Official FDA record: K261139
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.