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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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23 records meeting your search criteria returned- Product Code: OKS Product Problem: Use of Device Problem Report Date From: 01/1/2015
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ManufacturerBrand NameDate Report Received
KANEKA CORPORATION LACRIFAST 07/02/2019
KANEKA CORPORATION LACRIFAST 10/29/2017
KANEKA CORPORATION LACRIFAST 10/03/2017
KANEKA CORPORATION LACRIFAST 06/26/2017
KANEKA CORPORATION LACRIFAST 06/15/2017
KANEKA CORPORATION LACRIFAST 04/24/2017
KANEKA CORPORATION LACRIFAST 01/13/2017
KANEKA CORPORATION LACRIFAST 01/05/2017
KANEKA CORPORATION LACRIFAST 12/25/2016
KANEKA CORPORATION LACRIFAST 12/25/2016
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