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

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
1 to 10 of 12 Results
ProductCode: MDB Applicant: BIOMERIEUX, INC. Decision Date To: 09/18/2024
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 12 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
bact/alert mp reagent system bioMerieux, Inc. K190405 05/15/2019
bact/alert fa plus; bact/alert pf plus bioMerieux, Inc. K183166 02/11/2019
bact/alert virtuo microbial detection system, bact/alert virtuo, virtuo bioMerieux, Inc. K161816 03/28/2017
bact/alert fn plus culture bottle BIOMERIEUX, INC. K121455 01/25/2013
bact/alert pf plus culture bottle BIOMERIEUX, INC. K121446 01/25/2013
bact/alert fa plus culture bottle BIOMERIEUX, INC. K121461 01/22/2013
bact/alert mp culture bottles (plastic) BIOMERIEUX, INC. K031737 07/14/2003
bact/alert sn culture bottle BIOMERIEUX, INC. K021123 04/26/2002
bact/alert fn culture bottle BIOMERIEUX, INC. K020815 04/18/2002
bact/alert pf culture bottle BIOMERIEUX, INC. K020923 04/18/2002
-
-