• 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 K880434
Device Name MEDICOMP STRAIGHT SWIVEL ADAPTOR
Applicant
MEDICOMP, INC.
411 FREEMONT ST.
ANOKA,  MN  55303
Applicant Contact DUNCAN G JOHNSON
Correspondent
MEDICOMP, INC.
411 FREEMONT ST.
ANOKA,  MN  55303
Correspondent Contact DUNCAN G JOHNSON
Regulation Number868.5810
Classification Product Code
BZA  
Date Received02/01/1988
Decision Date 03/31/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-