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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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9 records meeting your search criteria returned- Product Code: LSZ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
VYAIRE MEDICAL 3100 HIGH FREQUENCY OSCILLATING VENTILAT 08/14/2023
VYAIRE MEDICAL INC. 3100 HIGH FREQUENCY OSCILLATING VENTILAT 03/09/2023
VYAIRE MEDICAL INC. 3100 HIGH FREQUENCY OSCILLATING VENTILAT 03/20/2022
VYAIRE MEDICAL 3100A VENTILATOR 10/23/2020
VYAIRE MEDICAL 3100 HIGH FREQUENCY OSCILLATING VENTILAT 04/10/2020
VYAIRE MEDICAL, INC 3100 HIGH FREQUENCY OSCILLATORY VENTILAT 12/22/2017
VYAIRE MEDICAL, INC 3100 HIGH FREQUENCY OSCILLATORY VENTILAT 12/18/2017
BUNNELL, INC. BUNNELL LIFE PULSE HIGH FREQUENCY VENTIL 08/17/2016
BUNNELL, INC. BUNNELL LIFEPULSE HIGH FREQUENCY VENTILA 05/26/2016
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