• 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 Reagents, Clostridium Difficile Toxin
510(k) Number K102242
Device Name OSOM C. DIFFICILE TOXIN A/B TEST
Applicant
GENZYME CORPORATION
31 NEW YORK AVENUE
FRAMINGHAM,  MA  01701
Applicant Contact CAROL C RYERSON
Correspondent
GENZYME CORPORATION
31 NEW YORK AVENUE
FRAMINGHAM,  MA  01701
Correspondent Contact CAROL C RYERSON
Regulation Number866.2660
Classification Product Code
LLH  
Date Received08/09/2010
Decision Date 12/21/2010
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
Recalls CDRH Recalls
-
-