Cleared Traditional

K192508 - Medsynapse Ris Pacs & Medsynapse VNA (FDA 510(k) Clearance)

Nov 2019
Decision
71d
Days
Class 2
Risk

K192508 is an FDA 510(k) clearance for the Medsynapse Ris Pacs & Medsynapse VNA. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).

Submitted by Medsynaptic Private, Ltd. (Shivaji Nagar, IN). The FDA issued a Cleared decision on November 22, 2019, 71 days after receiving the submission on September 12, 2019.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number K192508 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 12, 2019
Decision Date November 22, 2019
Days to Decision 71 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code LLZ - System, Image Processing, Radiological
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.2050