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 Connector, Airway (Extension)
510(k) Number K864896
Device Name MEDICOMP INHALANT MASK ELBOW
Applicant
MEDICOMP, INC.
ROUTE 3
PRINCETON,  MN  55371
Applicant Contact DUNCAN G JOHNSON
Correspondent
MEDICOMP, INC.
ROUTE 3
PRINCETON,  MN  55371
Correspondent Contact DUNCAN G JOHNSON
Regulation Number868.5810
Classification Product Code
BZA  
Date Received12/15/1986
Decision Date 02/20/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-