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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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281 records meeting your search criteria returned- Product Code: LIT Product Problem: Material Separation Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
KANEKA CORPORATION SHIDEN 07/10/2020
KANEKA CORPORATION DIVA 07/07/2020
KANEKA CORPORATION DIVA 07/07/2020
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 06/18/2020
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 06/12/2020
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 05/28/2020
KANEKA CORPORATION SHIRANUI HP 05/18/2020
KANEKA CORPORATION R2P CROSSTELLA RX 05/18/2020
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 04/24/2020
ABBOTT VASCULAR RX VIATRAC PLUS 04/17/2020
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