FDA 510(k) Application Details - K851202

Device Classification Name Complement C1q, Antigen, Antiserum, Control

  More FDA Info for this Device
510(K) Number K851202
Device Name Complement C1q, Antigen, Antiserum, Control
Applicant GILFORD
17392 DAIMLER ST.
IRVINE, CA US
Other 510(k) Applications for this Company
Contact RONALD D SCHAEFER
Other 510(k) Applications for this Contact
Regulation Number 866.5240

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

  More FDA Info for this Product Code
Date Received 03/26/1985
Decision Date 04/29/1985
Decision SE - Substantially Equivalent
Classification Advisory Committee IM - Immunology
Review Advisory Committee IM - Immunology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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