FDA 510(k) Application Details - K924020

Device Classification Name Apparatus, Electrophoresis, For Clinical Use

  More FDA Info for this Device
510(K) Number K924020
Device Name Apparatus, Electrophoresis, For Clinical Use
Applicant THE BINDING SITE, LTD.
WESTSIDE TOWERS, SUITE 1000
11845 WEST OLYMPIC BLVD.
LOS ANGELES, CA US
Other 510(k) Applications for this Company
Contact JAY H GELLER
Other 510(k) Applications for this Contact
Regulation Number 862.2485

  More FDA Info for this Regulation Number
Classification Product Code JJN
Other 510(k) Applications for this Device

  More FDA Info for this Product Code
Date Received 08/11/1992
Decision Date 12/28/1992
Decision SE - Substantially Equivalent
Classification Advisory Committee CH - Clinical Chemistry
Review Advisory Committee CH - Clinical Chemistry
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact