K234131
- 510(k) number
- K234131
- Device name
- Resolv Endoscopic Hemostat System
- Applicant
- Hemostasis, LLC MN · US
- Product code
- QAU — Hemostatic Device For Endoscopic Gastrointestinal Us
- Decision date
- 2024-07-26
- Date received
- 2023-12-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K234131.pdf
Official FDA record: K234131
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.