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 tubing, pressure and accessories
510(k) Number K790150
Device Name BIRD DRIVE LINE ADAPTOR
Applicant
AIRLIFE, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
AIRLIFE, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.5860
Classification Product Code
BYX  
Date Received01/12/1979
Decision Date 02/01/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-