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
-
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
 


New Search Back To Search Results
Device Classification Name c. difficile toxin gene amplification assay
510(k) Number K130470
Device Name BD MAX CDIFF ASSAY, BD MAX INSTRUMENT
Applicant
GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)
2555 Boul. du Parc-Technologique
Quebec,  CA G1P 4S5
Applicant Contact PATRICIA DIONNE
Correspondent
GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)
2555 Boul. du Parc-Technologique
Quebec,  CA G1P 4S5
Correspondent Contact PATRICIA DIONNE
Regulation Number866.3130
Classification Product Code
OZN  
Subsequent Product Code
OOI  
Date Received02/25/2013
Decision Date 04/02/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-