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 K882500
Device Name VAPORIZER, ANESTHESIA, NON-HEATED
Applicant
Anesthetic Vaporizer Services
10185 Main St.
Clarence,  NY  14031
Applicant Contact KEITH JONES
Correspondent
Anesthetic Vaporizer Services
10185 Main St.
Clarence,  NY  14031
Correspondent Contact KEITH JONES
Regulation Number868.5880
Classification Product Code
CAD  
Date Received06/17/1988
Decision Date 08/01/1988
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
-
-