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FDA 510(k)

FOURSIGHT VIEWTOOL IMAGE VIEWER

K-Number: K052895 · 2005-10-27

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2005-10-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FOURSIGHT VIEWTOOL IMAGE VIEWER 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 2005-10-27 under 510(k) number K052895. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOURSIGHT VIEWTOOL IMAGE VIEWER?

FOURSIGHT VIEWTOOL IMAGE VIEWER is a medical device that received FDA 510(k) clearance on 2005-10-27. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K052895.

When did FOURSIGHT VIEWTOOL IMAGE VIEWER receive FDA 510(k) clearance?

FOURSIGHT VIEWTOOL IMAGE VIEWER received FDA 510(k) clearance on 2005-10-27, under 510(k) number K052895.

Who is the listed applicant for FOURSIGHT VIEWTOOL IMAGE VIEWER?

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 FOURSIGHT VIEWTOOL IMAGE VIEWER?

The FDA product code for FOURSIGHT VIEWTOOL IMAGE VIEWER is LLZ.

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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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