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FDA 510(k)

SIEMENS INFINITY SC 6002XL MODIFICATIONS

K-Number: K020144 · 2002-02-15

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2002-02-15
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS INFINITY SC 6002XL MODIFICATIONS is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2002-02-15 under 510(k) number K020144. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS INFINITY SC 6002XL MODIFICATIONS?

SIEMENS INFINITY SC 6002XL MODIFICATIONS is a medical device that received FDA 510(k) clearance on 2002-02-15. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K020144.

When did SIEMENS INFINITY SC 6002XL MODIFICATIONS receive FDA 510(k) clearance?

SIEMENS INFINITY SC 6002XL MODIFICATIONS received FDA 510(k) clearance on 2002-02-15, under 510(k) number K020144.

Who is the listed applicant for SIEMENS INFINITY SC 6002XL MODIFICATIONS?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIEMENS INFINITY SC 6002XL MODIFICATIONS?

The FDA product code for SIEMENS INFINITY SC 6002XL MODIFICATIONS is DRT.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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