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

 
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403 records meeting your search criteria returned- Product Code: KPO Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
CORPORATE COLLECTIVE CONCENTRATE- BICARB 09/22/2017
CORPORATE COLLECTIVE CONCENTRATE- ACID 09/22/2017
MONTREAL LIQUID BICARBONATE 4000 FMC 3 BOT/CS 08/11/2017
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 08/10/2017
MEDIVATORS, INC. CENTRISOL LIQUID BICARBONATE CONCENTRATE 08/03/2017
IRVING MANUFACTURING PLANT NATURALYTE DRY PACK RX-12 07/12/2017
IRVING MANUFACTURING PLANT GRANUFLO 2251 2K 2.5CA 1MG 16.5 GAL 07/12/2017
OREGON MANUFACTURING PLANT NATURALYTE DRY PACK RX-12 06/26/2017
OREGON MANUFACTURING PLANT GRANUFLO 3251 3K 2.5CA 1MG 16.5 GAL 06/26/2017
CORPORATE COLLECTIVE CONCENTRATE- NATURALYTE 06/15/2017
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