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 Vaporizer, Anesthesia, Non-Heated
510(k) Number K861839
Device Name VAPOFIL
Applicant
SOUTHMEDIC, INC.
P.O. BOX 1365
BARRIE, ONTARIO CANADA,  CA L4M 5R4
Applicant Contact LEE MCDONALD
Correspondent
SOUTHMEDIC, INC.
P.O. BOX 1365
BARRIE, ONTARIO CANADA,  CA L4M 5R4
Correspondent Contact LEE MCDONALD
Regulation Number868.5880
Classification Product Code
CAD  
Date Received05/13/1986
Decision Date 05/21/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-