FDA 510(k) Application Details - K760850

Device Classification Name Gouge, Surgical, General & Plastic Surgery

  More FDA Info for this Device
510(K) Number K760850
Device Name Gouge, Surgical, General & Plastic Surgery
Applicant V. MUELLER O.V. BAXTER HEALTHCARE CORP.

, US
Other 510(k) Applications for this Company
Regulation Number 878.4800

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

  More FDA Info for this Product Code
Date Received 10/15/1976
Decision Date 11/03/1976
Decision SE - Substantially Equivalent
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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