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
-
1 to 2 of 2 Results
510(K) Number: K142953
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]
OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4 2 01/10/2022 FEI # 1000136533
Haag-Streit USA Inc
OCT-Camera 211 01 A1, Running software iOCT-Control 3 v1.4 2 01/10/2022 FEI # 1000136533
Haag-Streit USA Inc
-
-