Cios Flow

Interventional Fluoroscopic X-ray System

Siemens Medical Solutions USA, Inc.

The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Cios Flow.

Pre-market Notification Details

• Device ID: K203504
• 510k Number: K203504
• Device Name: Cios Flow
• Classification: Interventional Fluoroscopic X-ray System
• Applicant: Siemens Medical Solutions USA, Inc. 40 Liberty Boulevard 65-1A Malvern, PA 19355
• Contact: Cordell Fields
• Correspondent: Cordell Fields; Siemens Medical Solutions USA, Inc. 40 Liberty Boulevard 65-1A Malvern, PA 19355
• Product Code: OWB
• Subsequent Product Code: JAA
• Subsequent Product Code: OXO
• CFR Regulation Number: 892.1650 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Special
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2020-11-30
• Decision Date: 2020-12-22
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
04056869246628	K203504	000