510(k) K111543
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.