ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW
K-Number: K990093 · 1999-05-11
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Device Summary
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.
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
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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