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FDA 510(k)

SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS

K-Number: K023569 · 2002-11-04

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2002-11-04
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS MULTIVIEW WORKSTATION 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 2002-11-04 under 510(k) number K023569. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS?

SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS is a medical device that received FDA 510(k) clearance on 2002-11-04. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K023569.

When did SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS receive FDA 510(k) clearance?

SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS received FDA 510(k) clearance on 2002-11-04, under 510(k) number K023569.

Who is the listed applicant for SIEMENS MULTIVIEW WORKSTATION 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 MULTIVIEW WORKSTATION MODIFICATIONS?

The FDA product code for SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS is MHX.

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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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