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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
 

 
 
7 records meeting your search criteria returned- Product Code: LRC Product Problem: Burst Container or Vessel Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ACCLARENT, INC. RELIEVA ULTIRRA 05/17/2018
ACCLARENT, INC. RELIEVA SPINPLUS 07/18/2017
MEDTRONIC USA NUVENT 12/09/2016
ACCLARENT INC. RELIEVA SCOUT SINUS DILATION SYSTEM 01/04/2016
ACCLARENT ACCLARENT 05/22/2015
ACCLARENT INSPIRA AIR BALLOON 08/12/2014
ACCLARENT RELIEVA SPIN SINUPLASTY SYSTEM 03/03/2014
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