• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

OTC - Over The Counter

  • 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
Document NumberK051936
Test Name Taidoc Dr. T TD-3216 Blood Glucose and Blood Pressure Measurement System  
Manufacturer NameTaidoc Technology Corporation
Consumer Information Phone Number(703)591-4934
Test TypeGlucose monitoring devices (FDA cleared/home use)
Effective Date08/11/2005
Device Classification Name System, Test, Blood Glucose, Over The Counter
510(k) Number K051936
Device Name CLEVER CHECK TD-3215/DR. T TD-3216 BLOOD GLUCOSE AND BLOOD PRESSURE MEASUREMENT SYSTEMS
Applicant
Taidoc Technology Corporation
4f, 88, Sec. 1, Kwang Fu Rd.
San Chung, Taipei,  TW 241
Applicant Contact SHU-MEI WU
Correspondent
Taidoc Technology Corporation
4f, 88, Sec. 1, Kwang Fu Rd.
San Chung, Taipei,  TW 241
Correspondent Contact SHU-MEI WU
Regulation Number862.1345
Classification Product Code
NBW  
Date Received07/18/2005
Decision Date 08/08/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Statement Statement
FDA Review Decision Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-