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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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171 records meeting your search criteria returned- Product Code: IYO Product Problem: Application Program Freezes, Becomes Nonfunctional Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
Unknown Manufacturer SITE-RITE 8 ULTRASOUND 07/10/2020
Unknown Manufacturer SITE~RITE 8 ULTRASOUND SYSTEM 07/01/2020
Unknown Manufacturer REFURB, SR PREVUE PLUS 06/10/2020
Unknown Manufacturer SITE~RITE 8 ULTRASOUND SYSTEM CONSOLE WI 06/10/2020
Unknown Manufacturer SITE-RITE 8 ULTRASOUND 06/10/2020
BARD ACCESS SYSTEMS REFURB, SR PREVUE PLUS 06/10/2020
Unknown Manufacturer REFURB, SR PREVUE PLUS 06/09/2020
Unknown Manufacturer SITE~RITE 8 ULTRASOUND SYSTEM CONSOLE WI 06/09/2020
Unknown Manufacturer REFURB, SR PREVUE PLUS 05/28/2020
BARD ACCESS SYSTEMS SITE-RITE 8 ULTRASOUND SYSTSEM CONSOLE 05/28/2020
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