• 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 Chromatographic Separation, Cpk Isoenzymes
510(k) Number K791826
Device Name CPK CLINI GEL KIT
Applicant
Clinical Sciences, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Clinical Sciences, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number862.1215
Classification Product Code
JHT  
Date Received09/17/1979
Decision Date 10/01/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-