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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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69 records meeting your search criteria returned- Product Code: FDF Product Problem: Partial Blockage Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA II COLONOVIDEOSCOPE 03/10/2021
OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA III COLONOVIDEOSCOPE 02/17/2021
OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA II COLONOVIDEOSCOPE 01/14/2021
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 12/04/2020
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 11/13/2020
OLYMPUS CORPORATION OF THE AMERICAS EUS SCOPE 12/16/2016
OLYMPUS CORPORATION OF THE AMERICAS EVIS EXERA III 11/10/2016
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 07/07/2016
HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX 06/30/2016
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