K230645
- 510(k) number
- K230645
- Device name
- BeneHold Surgical Incise Drape with CHG antimicrobial II
- Applicant
- Avery Dennison Medical , Ltd. IE
- Product code
- KKX — Drape, Surgical, Antimicrobial
- Decision date
- 2023-10-25
- Date received
- 2023-03-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K230645
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.