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 Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine
510(k) Number K854971
Device Name V-TREND EIA T4 ENZYME IMMUNOASSAY TEST KIT
Applicant
V-Tech, Inc.
270 E. Bonita Ave.
Pomona,  CA  91767
Applicant Contact AILENE HERRANEN
Correspondent
V-Tech, Inc.
270 E. Bonita Ave.
Pomona,  CA  91767
Correspondent Contact AILENE HERRANEN
Regulation Number862.1700
Classification Product Code
KLI  
Date Received12/11/1985
Decision Date 02/06/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-