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 Electrode, Ion Specific, Calcium
510(k) Number K873345
Device Name 'MICROLYTE 4/5'
Applicant
Kone Instruments, Inc.
1110 W. Throndale Ave.
Benseville,  IL  60106
Applicant Contact KATHY SCHAEFER
Correspondent
Kone Instruments, Inc.
1110 W. Throndale Ave.
Benseville,  IL  60106
Correspondent Contact KATHY SCHAEFER
Regulation Number862.1145
Classification Product Code
JFP  
Date Received08/19/1987
Decision Date 09/11/1987
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
-
-