Devices · SIEMENS MEDICAL SOLUTIONS USA, INC.

YSIO MAX

SIEMENS MEDICAL SOLUTIONS USA, INC. is listed for YSIO MAX (K133259). The FDA list gives January 24, 2014 as the date of the final decision. The lead panel is Radiology, and the database link on the FDA list is the 510(k) pathway. The primary product code on the FDA list is KPR. openFDA did not return a classification record for that code in this copy of the data. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K133259

Official FDA database record

Date of final decision

January 24, 2014

Company on the FDA list

SIEMENS MEDICAL SOLUTIONS USA, INC.

Lead panel

Radiology

Primary product code

KPR

openFDA device name for the code

System, X-Ray, Stationary

Device class

2

Regulation number

892.1680

openFDA decision description

Substantially Equivalent

openFDA decision code

SESE

Statement or summary label

Summary