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 bag, bile collecting
510(k) Number K911129
Device Name MMG BILE BAG
Applicant
MEDICAL TECHNOLOGIES OF GEORGIA
5335 DIVIDEND DR.
DECATUR,  GA  30035
Applicant Contact TIMOTHY D GOLDEN
Correspondent
MEDICAL TECHNOLOGIES OF GEORGIA
5335 DIVIDEND DR.
DECATUR,  GA  30035
Correspondent Contact TIMOTHY D GOLDEN
Regulation Number876.5010
Classification Product Code
EXF  
Date Received03/14/1991
Decision Date 08/07/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-