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 conserver, oxygen
510(k) Number K992935
Device Name OCD2001
Applicant
CONTEMPORARY PRODUCTS, INC.
530 RIVERSIDE INDUSTRIAL PWKY.
PORTLAND,  ME  04103 -1066
Applicant Contact BARRY A SCHWARTZ
Correspondent
CONTEMPORARY PRODUCTS, INC.
530 RIVERSIDE INDUSTRIAL PWKY.
PORTLAND,  ME  04103 -1066
Correspondent Contact BARRY A SCHWARTZ
Regulation Number868.5905
Classification Product Code
NFB  
Date Received08/31/1999
Decision Date 06/20/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Abbreviated
Reviewed by Third Party No
Combination Product No
-
-