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 catheter, urethral
510(k) Number K871999
Device Name MMG URO-SELF CATHETER
Applicant
MEDICAL MARKETING GROUP
5335 DIVIDEND DR.
DECATUR,  GA  30035
Applicant Contact TIMOTHY D GOLDEN
Correspondent
MEDICAL MARKETING GROUP
5335 DIVIDEND DR.
DECATUR,  GA  30035
Correspondent Contact TIMOTHY D GOLDEN
Regulation Number876.5130
Classification Product Code
GBM  
Date Received05/26/1987
Decision Date 08/25/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-