510(k) K182564

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

K182564 is an FDA 510(k) premarket notification submitted by Quantib B.V. for the device "Quantib ND". The FDA issued a decision of Substantially Equivalent on December 27, 2018. 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
December 27, 2018
Date Received
September 18, 2018
Clearance Type
Traditional
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