510(k) K121350

VIRTUSO SYSTEM FOR IHC (DO-7) by Ventana Medical Systems, Inc. — Product Code NOT

K121350 is an FDA 510(k) premarket notification submitted by Ventana Medical Systems, Inc. for the device "VIRTUSO SYSTEM FOR IHC (DO-7)". The FDA issued a decision of Substantially Equivalent on June 1, 2012. 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
June 1, 2012
Date Received
May 4, 2012
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.