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FDA 510(k)

ZYMED TELEMETRY SYSTEM

K-Number: K980186 · 1998-10-07

ApplicantAgilent Technologies
Decision Date1998-10-07
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZYMED TELEMETRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies. It received FDA 510(k) clearance on 1998-10-07 under 510(k) number K980186. 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?

ZYMED TELEMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 1998-10-07. The listed applicant is Agilent Technologies. The 510(k) number is K980186.

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

ZYMED TELEMETRY SYSTEM received FDA 510(k) clearance on 1998-10-07, under 510(k) number K980186.

Who is the listed applicant for ZYMED TELEMETRY SYSTEM?

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?

The FDA product code for ZYMED TELEMETRY SYSTEM 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.

K0109492010 PLUS HOLTER FOR WINDOWSK0039402010 PLUS HOLTER FOR WINDOWSK0037632010 PLUS HOLTER FOR WINDOWSK001308MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEWK990093ZYMED TELEMETRY SYSTEM: MODEL EASIVIEWK942781DIGITAL HOLTER RECORDER

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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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