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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
 

 
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319 records meeting your search criteria returned- Product Code: DRA Patient Problem: No Patient Involvement Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 04/16/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 04/12/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 04/10/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 04/09/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 04/04/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 03/26/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 03/22/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 03/18/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 03/04/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 02/25/2019
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