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 Tube, Tracheal (W/Wo Connector)
510(k) Number K894669
Device Name LASER SHIELDING TUBE
Applicant
Vitaid, Ltd.
147 Old Orchard Grove
Toronto, Ontario, Canada
M5m 2e1,  CA
Applicant Contact WILLIAM G STEWART
Correspondent
Vitaid, Ltd.
147 Old Orchard Grove
Toronto, Ontario, Canada
M5m 2e1,  CA
Correspondent Contact WILLIAM G STEWART
Regulation Number868.5730
Classification Product Code
BTR  
Date Received07/24/1989
Decision Date 10/13/1989
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
-
-