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FDA 510(k)

1481 T DIGITAL TELEMETRY SYSTEMS, ENHANCED

K-Number: K945384 · 1995-05-10

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1995-05-10
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

1481 T DIGITAL TELEMETRY SYSTEMS, ENHANCED 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 1995-05-10 under 510(k) number K945384. 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 1481 T DIGITAL TELEMETRY SYSTEMS, ENHANCED?

1481 T DIGITAL TELEMETRY SYSTEMS, ENHANCED is a medical device that received FDA 510(k) clearance on 1995-05-10. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K945384.

When did 1481 T DIGITAL TELEMETRY SYSTEMS, ENHANCED receive FDA 510(k) clearance?

1481 T DIGITAL TELEMETRY SYSTEMS, ENHANCED received FDA 510(k) clearance on 1995-05-10, under 510(k) number K945384.

Who is the listed applicant for 1481 T DIGITAL TELEMETRY SYSTEMS, ENHANCED?

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 1481 T DIGITAL TELEMETRY SYSTEMS, ENHANCED?

The FDA product code for 1481 T DIGITAL TELEMETRY SYSTEMS, ENHANCED 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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