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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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11 records meeting your search criteria returned- Product Code: FDS Product Problem: Insufficient Flow or Under Infusion Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
AIZU OLYMPUS CO., LTD. EVIS EXERA III GASTROINTESTINAL VIDEOSCO 01/08/2024
AIZU OLYMPUS CO., LTD. EVIS LUCERA GASTROINTESTINAL VIDEOSCOPE 11/30/2023
AIZU OLYMPUS CO., LTD. EVIS LUCERA ELITE GASTROINTESTINAL VIDEO 08/31/2023
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 06/06/2023
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 06/06/2023
HOYA CORPORATION PENTAX PENTAX 06/05/2023
HOYA CORPORATION PENTAX PENTAX 06/05/2023
AIZU OLYMPUS CO., LTD. GASTROINTESTINAL VIDEOSCOPE 11/11/2022
OLYMPUS MEDICAL SYSTEMS CORP. GASTROINTESTINAL VIDEOSCOPE 10/10/2021
OLYMPUS MEDICAL SYSTEMS CORP. EVIS LUCERA ELITE GASTROINTESTINAL VIDEO 09/03/2021
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