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FDA 510(k)

SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM

K-Number: K900319 · 1990-06-28

ApplicantSiemens Medical Electronics
Decision Date1990-06-28
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Electronics. It received FDA 510(k) clearance on 1990-06-28 under 510(k) number K900319. 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 SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM?

SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 1990-06-28. The listed applicant is Siemens Medical Electronics. The 510(k) number is K900319.

When did SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM receive FDA 510(k) clearance?

SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM received FDA 510(k) clearance on 1990-06-28, under 510(k) number K900319.

Who is the listed applicant for SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM?

The FDA 510(k) record lists Siemens Medical Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM?

The FDA product code for SIEMENS SIRECUST 1481T, DIGITAL TELEMETRY SYSTEM is DSI.

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Other records listing Siemens Medical Electronics 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.

K935043SIEMENS CLINICAL WORK STATIONK921930SIEMENS SIRECUST 700 BEDSIDES/ACCESSORIES, MODIFIK920445SIEMENS SIRECUST PENTA SYSTEM AND ACCESSORIESK914765SIEMENS NP NONINVASIVE BLOOD PRESS MEASUREMENT SYSK912070SIEMENS RADIOTOM 904 & 904E ELECTROSURGERY UNITK913489SIEMENS MICRO2 PULSE OXIMETER

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Related Devices (Code: DSI)

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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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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