• 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 airway, oropharyngeal, anesthesiology
510(k) Number K760488
Device Name AIRWAY, DUAL CHANNEL
Applicant
HUDSON OXYGEN THERAPY SALES CO.
803 N. Front St. Suite 3
mchenry,  IL  60050
Correspondent
HUDSON OXYGEN THERAPY SALES CO.
803 N. Front St. Suite 3
mchenry,  IL  60050
Regulation Number868.5110
Classification Product Code
CAE  
Date Received08/20/1976
Decision Date 09/03/1976
Decision substantially equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-