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FDA 510(k)

ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW

K-Number: K990093 · 1999-05-11

Decision Date1999-05-11
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies. It received FDA 510(k) clearance on 1999-05-11 under 510(k) number K990093. 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 ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW?

ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW is a medical device that received FDA 510(k) clearance on 1999-05-11. The listed applicant is Agilent Technologies. The 510(k) number is K990093.

When did ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW receive FDA 510(k) clearance?

ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW received FDA 510(k) clearance on 1999-05-11, under 510(k) number K990093.

Who is the listed applicant for ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW?

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

What is the FDA product code for ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW?

The FDA product code for ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW is DSI.

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 Agilent Technologies 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: 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.

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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