FDA 510(k) Application Details - K926036

Device Classification Name Snare, Surgical

  More FDA Info for this Device
510(K) Number K926036
Device Name Snare, Surgical
Applicant ACUFEX MICROSURGICAL, INC.
130 FORBES BLVD.
MANSFIELD, MA US
Other 510(k) Applications for this Company
Contact LYNNE ARONSON
Other 510(k) Applications for this Contact
Regulation Number 878.4800

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

  More FDA Info for this Product Code
Date Received 12/01/1992
Decision Date 05/05/1993
Decision SE - Substantially Equivalent
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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