510(k) K221106

Quantib Prostate by Quantib B.V. — Product Code LLZ

K221106 is an FDA 510(k) premarket notification submitted by Quantib B.V. for the device "Quantib Prostate". The FDA issued a decision of Substantially Equivalent on May 13, 2022. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Quantib B.V. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 13, 2022
Date Received
April 15, 2022
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Image Processing, Radiological
Device Class
Class II
Regulation Number
892.2050
Review Panel
RA
Submission Type