• 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
-
-