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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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75 records meeting your search criteria returned- Product Code: LRC Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ATOS MEDICAL AB PROVOX BRUSH 09/25/2019
ATOS MEDICAL AB PROVOX BRUSH 04/11/2019
KARL STORZ SE & CO. KG HEYMAN NASAL SCISSORS 01/17/2019
MERIL LIFE SCIENCES PRIVATE LIMITED MESIRETM GUIDE- SINUS GUIDE CATHETER 01/03/2019
ACCLARENT, INC. INSPIRA AIR BALLOON DILATION SYSTEM, 14X 01/03/2019
MERIL LIFE SCIENCES PRIVATE LIMITED MESIRETM GUIDE- SINUS GUIDE CATHETER 01/02/2019
ATOS MEDICAL AB PROVOX BRUSH 12/18/2018
ACCLARENT, INC. RELIEVA FLEX SINUS GUIDE CATHETER, F-70C 11/21/2018
MEDTRONIC XOMED INC. NUVENT¿ 11/07/2018
ACCLARENT, INC. RELIEVA SPIN PLUS KIT, 3 GUIDES, 6MM, 5P 10/22/2018
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