• 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 ventilator, continuous, facility use
510(k) Number K901448
Device Name VEOLAR VENTILATOR
Applicant
HAMILTON MEDICAL, INC.
P.O. BOX 30008
RENO,  NV  89520
Applicant Contact TIM COWART
Correspondent
HAMILTON MEDICAL, INC.
P.O. BOX 30008
RENO,  NV  89520
Correspondent Contact TIM COWART
Regulation Number868.5895
Classification Product Code
CBK  
Date Received03/28/1990
Decision Date 12/20/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-