• 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, minimal ventilatory support, facility use
510(k) Number K974539
Device Name SULLIVAN VPAP II ST VENTILATORY SUPPORT SYSTEM
Applicant
RESMED LTD.
10121 CARROLL CANYON RD.
SAN DIEGO,  CA  92131
Applicant Contact SCOTT DUDEVOIR
Correspondent
RESMED LTD.
10121 CARROLL CANYON RD.
SAN DIEGO,  CA  92131
Correspondent Contact SCOTT DUDEVOIR
Regulation Number868.5895
Classification Product Code
MNT  
Date Received12/03/1997
Decision Date 08/06/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-