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 Absorber, Carbon-Dioxide
510(k) Number K843422
Device Name OHMEDA BAIN CIRCUIT ADAPTER GMS ABSOR
Applicant
Ohmeda Medical
P.O. Box 7550
Madison,  WI  53707
Applicant Contact RAYMOND T RIDDLE
Correspondent
Ohmeda Medical
P.O. Box 7550
Madison,  WI  53707
Correspondent Contact RAYMOND T RIDDLE
Regulation Number868.5310
Classification Product Code
BSF  
Date Received08/31/1984
Decision Date 10/23/1984
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
-
-