• 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 K952751
Device Name BIOCIRCUITS IOS T4/TU TEST CARTRIDGES
Applicant
Biocircuits Corp.
1324 Chesapeake Terr.
Sunnyvale,  CA  94089
Applicant Contact SHEILA J RAMERMAN
Correspondent
Biocircuits Corp.
1324 Chesapeake Terr.
Sunnyvale,  CA  94089
Correspondent Contact SHEILA J RAMERMAN
Regulation Number862.1700
Classification Product Code
KLI  
Subsequent Product Codes
JJY   KHQ  
Date Received06/15/1995
Decision Date 11/20/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-