BeneHold™ Surgical Incise Drape with CHG antimicrobial II
K-Number: K230645 · 2023-10-25
Device Summary
Frequently Asked Questions
What is the BeneHold™ Surgical Incise Drape with CHG antimicrobial II?
BeneHold™ Surgical Incise Drape with CHG antimicrobial II is a medical device that received FDA 510(k) clearance on 2023-10-25. The listed applicant is Avery Dennison Medical , Ltd.. The 510(k) number is K230645.
When did BeneHold™ Surgical Incise Drape with CHG antimicrobial II receive FDA 510(k) clearance?
BeneHold™ Surgical Incise Drape with CHG antimicrobial II received FDA 510(k) clearance on 2023-10-25, under 510(k) number K230645.
Who is the listed applicant for BeneHold™ Surgical Incise Drape with CHG antimicrobial II?
The FDA 510(k) record lists Avery Dennison Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BeneHold™ Surgical Incise Drape with CHG antimicrobial II?
The FDA product code for BeneHold™ Surgical Incise Drape with CHG antimicrobial II is KKX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KKX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.