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FDA 510(k)

MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW

K-Number: K001308 · 2000-05-17

ApplicantAgilent Technologies
Decision Date2000-05-17
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO 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 2000-05-17 under 510(k) number K001308. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW?

MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW is a medical device that received FDA 510(k) clearance on 2000-05-17. The listed applicant is Agilent Technologies. The 510(k) number is K001308.

When did MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW receive FDA 510(k) clearance?

MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW received FDA 510(k) clearance on 2000-05-17, under 510(k) number K001308.

Who is the listed applicant for MODIFICATION TO 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 MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW?

The FDA product code for MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW is DQA.

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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.

K0109492010 PLUS HOLTER FOR WINDOWSK0039402010 PLUS HOLTER FOR WINDOWSK0037632010 PLUS HOLTER FOR WINDOWSK990093ZYMED TELEMETRY SYSTEM: MODEL EASIVIEWK980186ZYMED TELEMETRY SYSTEMK942781DIGITAL HOLTER RECORDER

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Related Devices (Code: DQA)

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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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