• 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, non-continuous (respirator)
510(k) Number K974879
Device Name MODEL 7410 VOYAGER
Applicant
HEALTHDYNE TECHNOLOGIES, INC.
1850 PARKWAY PLACE
MARIETTA,  GA  30067
Applicant Contact TIMOTHY Y COWART
Correspondent
HEALTHDYNE TECHNOLOGIES, INC.
1850 PARKWAY PLACE
MARIETTA,  GA  30067
Correspondent Contact TIMOTHY Y COWART
Regulation Number868.5905
Classification Product Code
BZD  
Date Received12/30/1997
Decision Date 06/29/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-