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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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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115 records meeting your search criteria returned- Product Code: DRA Product Problem: Deformation Due to Compressive Stress Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 12/07/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 11/03/2020
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 10/01/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 09/17/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 08/27/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 08/17/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 08/05/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 07/17/2020
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 07/01/2020
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 05/18/2020
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