510(k) K931979

VENTANA NEGATIVE CONTROL REAGENT by Ventana Medical Systems, Inc. — Product Code DEM

K931979 is an FDA 510(k) premarket notification submitted by Ventana Medical Systems, Inc. for the device "VENTANA NEGATIVE CONTROL REAGENT". The FDA issued a decision of Substantially Equivalent on March 30, 1994. The device falls under product code DEM (Alpha-1-Antitrypsin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5130. Ventana Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 30, 1994
Date Received
April 22, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Alpha-1-Antitrypsin, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5130
Review Panel
IM
Submission Type