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FDA 510(k)

SIEMENS MULTI VIEW INFINITY TELEMETRY SYSTEM

K-Number: K024108 · 2002-12-18

Decision Date2002-12-18
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS MULTI VIEW INFINITY TELEMETRY SYSTEM 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 2002-12-18 under 510(k) number K024108. 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 MULTI VIEW INFINITY TELEMETRY SYSTEM?

SIEMENS MULTI VIEW INFINITY TELEMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 2002-12-18. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K024108.

When did SIEMENS MULTI VIEW INFINITY TELEMETRY SYSTEM receive FDA 510(k) clearance?

SIEMENS MULTI VIEW INFINITY TELEMETRY SYSTEM received FDA 510(k) clearance on 2002-12-18, under 510(k) number K024108.

Who is the listed applicant for SIEMENS MULTI VIEW INFINITY TELEMETRY SYSTEM?

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 MULTI VIEW INFINITY TELEMETRY SYSTEM?

The FDA product code for SIEMENS MULTI VIEW INFINITY TELEMETRY SYSTEM is MHX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Siemens Medical Solutions USA, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: MHX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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