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 Differential Rate Kinetic Method, Cpk Or Isoenzymes
510(k) Number K962126
Device Name ACS CKMB II IMMUNOASSAY
Applicant
Ciba Corning Diagnostics Corp.
17392 Daimler St.
Irvine,  CA  92714
Applicant Contact THOMAS F FLYNN
Correspondent
Ciba Corning Diagnostics Corp.
17392 Daimler St.
Irvine,  CA  92714
Correspondent Contact THOMAS F FLYNN
Regulation Number862.1215
Classification Product Code
JHS  
Subsequent Product Code
JHX  
Date Received06/03/1996
Decision Date 06/21/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-