• 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 instrumentation for clinical multiplex test systems
510(k) Number K110786
Device Name ESENSOR WARFARIN SENSITIVITY SALIVA TEST
Applicant
GENMARK DIAGNOSTICS, INC
5964 LA PLACE COURT
SUITE 100
CARLSBAD,  CA  92008
Applicant Contact JOHN RIOLO
Correspondent
GENMARK DIAGNOSTICS, INC
5964 LA PLACE COURT
SUITE 100
CARLSBAD,  CA  92008
Correspondent Contact JOHN RIOLO
Regulation Number862.2570
Classification Product Code
NSU  
Subsequent Product Codes
ODV   ODW  
Date Received03/22/2011
Decision Date 12/02/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-