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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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217 records meeting your search criteria returned- Product Code: PKL Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
HANGZHOU AGS MEDTECH CO., LTD. REPLAY 11/22/2023
BOSTON SCIENTIFIC CORPORATION RESOLUTION 360 ULTRA CLIP 11/21/2023
BOSTON SCIENTIFIC CORPORATION RESOLUTION CLIP 11/20/2023
BOSTON SCIENTIFIC CORPORATION RESOLUTION CLIP 11/17/2023
BOSTON SCIENTIFIC CORPORATION RESOLUTION 360 CLIP 11/16/2023
BOSTON SCIENTIFIC CORPORATION RESOLUTION 360 CLIP 11/16/2023
BOSTON SCIENTIFIC CORPORATION RESOLUTION 360 CLIP 11/15/2023
BOSTON SCIENTIFIC CORPORATION MANTIS 11/14/2023
BOSTON SCIENTIFIC CORPORATION RESOLUTION 360 CLIP 11/08/2023
BOSTON SCIENTIFIC CORPORATION RESOLUTION CLIP 11/06/2023
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