510(k) K210850

ADAS 3D by Adas3D Medical S.L. — Product Code LLZ

K210850 is an FDA 510(k) premarket notification submitted by Adas3D Medical S.L. for the device "ADAS 3D". The FDA issued a decision of Substantially Equivalent on April 5, 2021. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Adas3D Medical S.L. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 5, 2021
Date Received
March 22, 2021
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