ADMIRE

System, X-ray, Tomography, Computed

SIEMENS MEDICAL SYSTEMS, INC.

The following data is part of a premarket notification filed by Siemens Medical Systems, Inc. with the FDA for Admire.

Pre-market Notification Details

• Device ID: K133646
• 510k Number: K133646
• Device Name: ADMIRE
• Classification: System, X-ray, Tomography, Computed
• Applicant: SIEMENS MEDICAL SYSTEMS, INC. 51 VALLEY STREAM PARKWAY Malvern, PA 19301
• Contact: Kimberly Mangum
• Correspondent: Kimberly Mangum; SIEMENS MEDICAL SYSTEMS, INC. 51 VALLEY STREAM PARKWAY Malvern, PA 19301
• Product Code: JAK
• CFR Regulation Number: 892.1750 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2013-11-27
• Decision Date: 2014-06-20
• Summary: summary