• 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, Ph, Stomach
510(k) Number K871921
Device Name GENERAL PURPOSE COMBINATION PH ELECTRODE
Applicant
CHEMFET CORP.
777-108TH AVE. N.E. (1200)
RAINIER BANK PLAZA
BELLEVUE,  WA  98004
Applicant Contact LORI CADWELL
Correspondent
CHEMFET CORP.
777-108TH AVE. N.E. (1200)
RAINIER BANK PLAZA
BELLEVUE,  WA  98004
Correspondent Contact LORI CADWELL
Regulation Number876.1400
Classification Product Code
FFT  
Date Received05/18/1987
Decision Date 10/20/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-