• 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 Conserver, Oxygen
510(k) Number K022865
Device Name 6203
Applicant
CONTEMPORARY PRODUCTS, INC.
470 RIVERSIDE ST.
PORTLAND,  ME  04103
Applicant Contact BARRY A SCHWARTZ
Correspondent
CONTEMPORARY PRODUCTS, INC.
470 RIVERSIDE ST.
PORTLAND,  ME  04103
Correspondent Contact BARRY A SCHWARTZ
Regulation Number868.5905
Classification Product Code
NFB  
Date Received08/28/2002
Decision Date 02/13/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-