• 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 K983459
Device Name PULSED OXYGEN CONSERVING DEVICE, POCD
Applicant
MEDICAL ELECTRONIC DEVICES, INC.
2807 OREGON CT. #D6
TORRANCE,  CA  90503
Applicant Contact THOMAS WENZEL
Correspondent
MEDICAL ELECTRONIC DEVICES, INC.
2807 OREGON CT. #D6
TORRANCE,  CA  90503
Correspondent Contact THOMAS WENZEL
Regulation Number868.5905
Classification Product Code
NFB  
Date Received09/30/1998
Decision Date 12/08/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-