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FDA 510(k)

SIEMENS MULTIVIEW INFINITY TELEMETRY SYSTEM

K-Number: K003179 · 2000-11-09

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2000-11-09
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS MULTIVIEW 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 2000-11-09 under 510(k) number K003179. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS MULTIVIEW INFINITY TELEMETRY SYSTEM?

SIEMENS MULTIVIEW INFINITY TELEMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 2000-11-09. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K003179.

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

SIEMENS MULTIVIEW INFINITY TELEMETRY SYSTEM received FDA 510(k) clearance on 2000-11-09, under 510(k) number K003179.

Who is the listed applicant for SIEMENS MULTIVIEW 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 MULTIVIEW INFINITY TELEMETRY SYSTEM?

The FDA product code for SIEMENS MULTIVIEW INFINITY TELEMETRY SYSTEM is DSI.

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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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