FDA 510(k), K222578, 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)

FDA 510(k), K222578, 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)

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510(K) Number: K222578
Device Name: 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)
Manufacturer: Hilary Hovde
Device Classification Name: Drape, Surgical
Regulation Number: KKX
Classification Product Code: 08/25/2022
Date Received: 05/18/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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