• 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 spatula, cervical, cytological
510(k) Number K983599
Device Name SAFETEX CHLAMYDIA TRACHOMATIS SPECIMEN COLLECTION KIT
Applicant
ANDWIN SCIENTIFIC
6636 VARIEL AVE.
CANOGA PARK,  CA  91303
Applicant Contact NATALIE SARRAF
Correspondent
ANDWIN SCIENTIFIC
6636 VARIEL AVE.
CANOGA PARK,  CA  91303
Correspondent Contact NATALIE SARRAF
Regulation Number884.4530
Classification Product Code
HHT  
Subsequent Product Code
LIO  
Date Received10/14/1998
Decision Date 12/11/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Microbiology
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-