FDA 510(k) Application Details - K002168

Device Classification Name Syringe, Cartridge

  More FDA Info for this Device
510(K) Number K002168
Device Name Syringe, Cartridge
Applicant RONVIG INSTRUMENTS, LTD.
GL.VEJLEVEJ 57-59
DK-8721 DAUGAARD DK-8721 DK
Other 510(k) Applications for this Company
Contact ANNETTE RAVN NEILSEN
Other 510(k) Applications for this Contact
Regulation Number 872.6770

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

  More FDA Info for this Product Code
Date Received 07/17/2000
Decision Date 10/13/2000
Decision SESE - SUBST EQUIV
Classification Advisory Committee DE - Dental
Review Advisory Committee DE - Dental
Statement / Summary / Purged Status Statement
Type Abbreviated
Reviewed By Third Party N
Expedited Review



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