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, ph, stomach
510(k) Number K853280
Device Name FOUR CHANNEL PH PROBE
Applicant
AKRON CITY HOSPITAL
AKRON,  OH  44309
Applicant Contact VINCENT J GRECZANIK
Correspondent
AKRON CITY HOSPITAL
AKRON,  OH  44309
Correspondent Contact VINCENT J GRECZANIK
Regulation Number876.1400
Classification Product Code
FFT  
Date Received08/05/1985
Decision Date 12/02/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-