• 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 Kit, Screening, Trichomonas
510(k) Number K020226
Device Name XENOSTRIP-TV TRICHOMONAS DIAGNOSTIC TEST KIT; CATALOG NUMBERS S1383.01, S1383.02 & S1383.03
Applicant
Hellen Professional Services
9418 Lasaine Ave.
Northridge,  CA  91325
Applicant Contact ROBIN HELLEN
Correspondent
Hellen Professional Services
9418 Lasaine Ave.
Northridge,  CA  91325
Correspondent Contact ROBIN HELLEN
Regulation Number866.2660
Classification Product Code
JWZ  
Date Received01/22/2002
Decision Date 08/22/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized
No
-
-