MAGNETOM VERIO

System, Nuclear Magnetic Resonance Imaging

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 Magnetom Verio.

Pre-market Notification Details

• Device ID: K072237
• 510k Number: K072237
• Device Name: MAGNETOM VERIO
• Classification: System, Nuclear Magnetic Resonance Imaging
• Applicant: SIEMENS MEDICAL SOLUTIONS USA, INC. 51 VALLEY STREAM PKWY. Malvern, PA 19355 -1406
• Contact: Judith Campbell
• Correspondent: Judith Campbell; SIEMENS MEDICAL SOLUTIONS USA, INC. 51 VALLEY STREAM PKWY. Malvern, PA 19355 -1406
• Product Code: LNH
• CFR Regulation Number: 892.1000 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2007-08-13
• Decision Date: 2007-10-10
• Summary: summary