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 System, Gastrointestinal Motility (Electrical)
510(k) Number K880581
Device Name AMBUL. PH & MOTILITY RECORDER FOR MEASURE OF PARA.
Applicant
Synectics-Dantec
1425 Greenway Dr.
Suite 600
Irving,  TX  75038
Applicant Contact MARIA LENDAU
Correspondent
Synectics-Dantec
1425 Greenway Dr.
Suite 600
Irving,  TX  75038
Correspondent Contact MARIA LENDAU
Regulation Number876.1725
Classification Product Code
FFX  
Date Received02/10/1988
Decision Date 08/11/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-