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 K923265
Device Name FUNNEL ADAPTOR
Applicant
Southmedic, Inc.
P.O. Box 1365
Barrie, Ontario Canada,  CA L4M 5R4
Applicant Contact PAUL E DRYDEN
Correspondent
Southmedic, Inc.
P.O. Box 1365
Barrie, Ontario Canada,  CA L4M 5R4
Correspondent Contact PAUL E DRYDEN
Regulation Number868.5880
Classification Product Code
CAD  
Date Received07/02/1992
Decision Date 03/18/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-