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 unit, liquid-oxygen, portable
510(k) Number K872449
Device Name NOMAD (BASE UNIT/PORTABLE UNIT)
Applicant
MINNESOTA VALLEY ENGINEERING, INC.
407 SEVENTH ST. N.W.
P.O. BOX 234
NEW PRAGUE,  MN  56071
Applicant Contact SCHOENBAUER
Correspondent
MINNESOTA VALLEY ENGINEERING, INC.
407 SEVENTH ST. N.W.
P.O. BOX 234
NEW PRAGUE,  MN  56071
Correspondent Contact SCHOENBAUER
Regulation Number868.5655
Classification Product Code
BYJ  
Date Received06/23/1987
Decision Date 07/21/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-