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 Conserver, Oxygen
510(k) Number K861199
Device Name BUNN MODEL 22 OXYGEN FLOW CONTROLLER
Applicant
THE JOHN BUNN CO.
290 CREEKSIDE DR.
TONAWANDA,  NY  14150
Applicant Contact DENNIS KENYON
Correspondent
THE JOHN BUNN CO.
290 CREEKSIDE DR.
TONAWANDA,  NY  14150
Correspondent Contact DENNIS KENYON
Regulation Number868.5905
Classification Product Code
NFB  
Date Received03/31/1986
Decision Date 08/26/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-