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
-
31 to 40 of 45 Results
510(K) Number: K023984
 < 
 1 
 2 
 3 
 4 
 5 
 > 
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]
Bronchofiberscope BF-P40 2 09/29/2018 Olympus Corporation of the Americas
Bronchovideoscope BF-P240 2 09/29/2018 Olympus Corporation of the Americas
Bronchovideoscope BF-P160 2 09/29/2018 Olympus Corporation of the Americas
Bronchovideoscope BF-MP60 2 09/29/2018 Olympus Corporation of the Americas
Bronchovideoscope BF-MP160F 2 09/29/2018 Olympus Corporation of the Americas
Bronchofibercope BF-6C240 2 09/29/2018 Olympus Corporation of the Americas
Bronchofiberscope BF-40 2 09/29/2018 Olympus Corporation of the Americas
Bronchovideoscope BF-3C40 2 09/29/2018 Olympus Corporation of the Americas
Bronchovideoscope BF-3C160 2 09/29/2018 Olympus Corporation of the Americas
Bronchovideoscope BF-240 2 09/29/2018 Olympus Corporation of the Americas
-
-