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510(k) Premarket Notification

Device Classification Name: mask, surgical: 510(k) Number: K173062: Device Name: Non Woven Face Mask (Models: VQN0185W (earloop) and VQN0185B (ties)) Applicant

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510(k) Premarket Notification - accessdata.fda.gov

non woven face mask (models: vqn0185w (earloop) and vqn0185b (ties)) V&Q Manufacturing Corporation K173062: 01/25/2018: surgical earloop face mask with bottom gap shield and surgical tie-on face mask with bottom gap shield: Prestige Ameritech K171162: 08/15/2017 - -

(Mask, Surgical) - FDA 510(k) Applications Database

FDA 510(k) Number: Applicant: Device Name: Decision Date: K910182: 3M COMPANY: 3M BRAND EAR LOOP FACE MASK, 2000F: 03/04/1991: K955382: 3M COMPANY: 3M MODEL 1860 HEALTH CARE PARTICULATE RESPIRATOR TYPE N95

January 25, 2018 Feiying Drug ... - accessdata.fda.gov

Non Woven Face Mask (Models: VQN0185W (earloop) and VQN0185B (ties)) is intended for single use by operating room personnel and other general healthcare workers to protect both patients and healthcare workers against transfer of microorganisms, blood and body fluids, and particulate materials.

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510K Summary - Food and Drug Administration

These face masks are intended for use in infection control practices to reduce the potential exposure of the wearer to blood and body fluids. The Kimberly-Clark, KC200 and KC300 face mask(s) is a single use, disposable device(s), provided non-sterile. 510(k) Number: Ki .

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