Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Medical Device Recalls
  • Print
  • Share
  • E-mail
-
11 to 17 of 17 Results
510(K) Number: K093514
 < 
 1 
 2 
 
Results per Page
New Searchexport reports to excelExport to Excel | HelpHelp
Product Description
Sort by Product Name [A-Z]
Sort by Product Name [Z-A]
Recall
Class
Sort by Recall Class [0-9]
Sort by Recall Class [9-0]
FDA Recall
Posting Date
Sort by Date Classified [0-9]
Sort by Date Classified [9-0]
Recalling Firm
Sort by Recalling Firm [A-Z]
Sort by Recalling Firm [Z-A]
Discovery NM/CT 670 ES, model 5376204-70-57 2 12/13/2018 GE Healthcare, LLC
Discovery NM/CT 670 DR, model 5376204-70-56 intended for use in detecting, localizing, diagnosing o... 2 12/13/2018 GE Healthcare, LLC
Discovery NM/CT 670 Pro, model 5376204-70-54 2 12/13/2018 GE Healthcare, LLC
GE Healthcare Discovery NM/CT 670. 670 Pro, 670 ES X-ray system 2 06/12/2017 GE Healthcare, LLC
GE Healthcare Discovery NMCT 670, Discovery NM 630, Optima NMCT 640, & Brivo NM 615. The GE Disco... 2 11/20/2013 GE Healthcare, LLC
GE Discovery NM/CT670; GE Discovery NM 630 Product Usage: a medical tool intended for use by a... 2 10/23/2012 GE Healthcare, LLC
GE Discovery NM/CT 670 The GE Discovery NM/CT 670 system is a medical tool intended for use by ap... 2 02/27/2012 GE Healthcare, LLC
-
-