FDA 510(k) Applications Submitted by Marty D Paugh

FDA 510(k) Number	Submission Date	Device Name	Applicant
K242664	09/04/2024	gentleheel« Adult Incision Device	GRI-Alleset, Inc.
K210131	01/19/2021	ComfortGuard Surgical Isolation Gown	GRI-Alleset, Inc
K220917	03/30/2022	gentleheel Micro-Preemie, gentleheel Preemie, gentleheel Newborn, gentleheel Toddler	GRI-Alleset, Inc.
K172712	09/08/2017	gentleheel Micro-Preemie, gentleheel Preemie, gentleheel Newborn, gentleheel Toddler	GRI Medical & Electronic Technology Co, Ltd