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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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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
OREGON MANUFACTURING PLANT NATURALYTE 2251 2K 2.5CA 1MG 55 GAL 12/21/2018
CONCORD MANUFACTURING 2008T GEN 2 BIBAG WITHOUT CDX 10/16/2018
CONCORD MANUFACTURING 2008T GEN 2 BIBAG WITHOUT CDX 07/16/2018
CORPORATE COLLECTIVE CONCENTRATE- NATURALYTE 04/25/2018
OREGON MANUFACTURING PLANT NATURALYTE DRY PACK RX-12 04/19/2018
OREGON MANUFACTURING PLANT NATURALYTE DRY PACK RX-12 04/18/2018
OREGON MANUFACTURING PLANT NATURALYTE DRY PACK RX-12 04/18/2018
OREGON MANUFACTURING PLANT NATURALYTE DRY PACK RX-12 04/18/2018
OREGON MANUFACTURING PLANT NATURALYTE DRY PACK RX-12 04/18/2018
OREGON MANUFACTURING PLANT NATURALYTE DRY PACK RX-12 04/18/2018
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