510(k) K941170

VENTANA ANTI-MELANOMA PRIMARY ANTIBODY by Ventana Medical Systems, Inc. — Product Code DEH

K941170 is an FDA 510(k) premarket notification submitted by Ventana Medical Systems, Inc. for the device "VENTANA ANTI-MELANOMA PRIMARY ANTIBODY". The FDA issued a decision of Substantially Equivalent on April 22, 1997. The device falls under product code DEH (Lambda, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5550. Ventana Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 22, 1997
Date Received
March 14, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lambda, Antigen, Antiserum, Control
Device Class
Class II
Regulation Number
866.5550
Review Panel
IM
Submission Type