K251238
- 510(k) number
- K251238
- Device name
- Vasoview Hemopro 3 Endoscopic Vessel Harvesting System (VH-6000); Vasoview Hemopro 3 Endoscopic Vessel Harvesting System with Vasoshield (VH-6001); Vasoview Hemopro 3 Power Supply (VH-6010)
- Applicant
- Maquet Cardiovascular, LLC NJ · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-05-30
- Date received
- 2025-04-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K251238.pdf
Official FDA record: K251238
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.