• 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 NumberK965184
Test Name WYNTEK DIAGNOSTICS PERFECTA PREGNANCY TEST  
Manufacturer NameWyntek Diagnostics, Inc.
Consumer Information Phone NumberNO PHONE NUMBER
Test TypeUrine hCG by visual color comparison tests
Effective Date02/04/1997
Device Classification Name Kit, Test, Pregnancy, Hcg, Over The Counter
510(k) Number K965184
Device Name PERFECTA PREGNANCY TEST
Applicant
Wyntek Diagnostics, Inc.
6146 Nancy Ridge Dr.,
Suite 101
San Diego,  CA  92121
Applicant Contact SHU-CHING CHENG
Correspondent
Wyntek Diagnostics, Inc.
6146 Nancy Ridge Dr.,
Suite 101
San Diego,  CA  92121
Correspondent Contact SHU-CHING CHENG
Regulation Number862.1155
Classification Product Code
LCX  
Date Received12/24/1996
Decision Date 02/04/1997
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
-
-