FDA 510(k)

BeneHold Surgical Incise Drape with CHG antimicrobial II

K-Number: K230645 · 2023-10-25

Decision Date2023-10-25

Product CodeKKX

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BeneHold Surgical Incise Drape with CHG antimicrobial II is a medical device manufactured by Avery Dennison Medical , Ltd.. It received FDA 510(k) clearance on 2023-10-25 under approval number K230645. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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. It is manufactured by Avery Dennison Medical , Ltd.. The 510(k) number is K230645.

When was BeneHold Surgical Incise Drape with CHG antimicrobial II approved by the FDA?

BeneHold Surgical Incise Drape with CHG antimicrobial II received FDA 510(k) clearance on 2023-10-25, under approval number K230645.

What company makes BeneHold Surgical Incise Drape with CHG antimicrobial II?

BeneHold Surgical Incise Drape with CHG antimicrobial II is manufactured by Avery Dennison Medical , Ltd..

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.

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Related Devices (Code: KKX)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.