510(k) K111543

VIRTUOSO (TM) SYSTEM FOR IHC HER2 (4B5) by Ventana Medical Systems, Inc. — Product Code NOT

K111543 is an FDA 510(k) premarket notification submitted by Ventana Medical Systems, Inc. for the device "VIRTUOSO (TM) SYSTEM FOR IHC HER2 (4B5)". The FDA issued a decision of Substantially Equivalent on October 12, 2011. The device falls under product code NOT (Microscope, Automated, Image Analysis, Operator Intervention), a Class II device regulated under 21 CFR 864.1860. Ventana Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 12, 2011
Date Received
June 2, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Microscope, Automated, Image Analysis, Operator Intervention
Device Class
Class II
Regulation Number
864.1860
Review Panel
PA
Submission Type

Automated microscopic immunohistochemistry image-analysis system to measure cell membrane intensity and pattern with operator intervention.