510(k) K192692

Brainomix 360 e-CTA by Brainomix Limited — Product Code LLZ

K192692 is an FDA 510(k) premarket notification submitted by Brainomix Limited for the device "Brainomix 360 e-CTA". The FDA issued a decision of Substantially Equivalent on May 28, 2020. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Brainomix Limited has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 28, 2020
Date Received
September 26, 2019
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