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FDA 510(k)

ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY)

K-Number: K924672 · 1992-12-15

ApplicantAgilent Technologies
Decision Date1992-12-15
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY) is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies. It received FDA 510(k) clearance on 1992-12-15 under 510(k) number K924672. 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 MONITOR MODEL T8010 (PRELIMINARY)?

ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY) is a medical device that received FDA 510(k) clearance on 1992-12-15. The listed applicant is Agilent Technologies. The 510(k) number is K924672.

When did ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY) receive FDA 510(k) clearance?

ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY) received FDA 510(k) clearance on 1992-12-15, under 510(k) number K924672.

Who is the listed applicant for ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY)?

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 MONITOR MODEL T8010 (PRELIMINARY)?

The FDA product code for ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY) is DSI.

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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.

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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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