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 Tubing, Pressure And Accessories
510(k) Number K863912
Device Name THE MMG 5 IN 1 CONNECTOR
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 Number868.5860
Classification Product Code
BYX  
Date Received10/08/1986
Decision Date 10/27/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-