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 Computer, Diagnostic, Pre-Programmed, Single-Function
510(k) Number K861437
Device Name QMED SYSTEM 2150
Applicant
Qmed, Inc.
5470 NW Innisbrook Pl.
Portland,  OR  97229
Applicant Contact DONALD L DUNSTAN
Correspondent
Qmed, Inc.
5470 NW Innisbrook Pl.
Portland,  OR  97229
Correspondent Contact DONALD L DUNSTAN
Regulation Number870.1435
Classification Product Code
DXG  
Date Received04/17/1986
Decision Date 05/20/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-