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FDA 510(k)

TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM

K-Number: K021447 · 2002-05-22

ApplicantAerotel Medical Systems (1998) , Ltd.
Decision Date2002-05-22
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aerotel Medical Systems (1998) , Ltd.. It received FDA 510(k) clearance on 2002-05-22 under 510(k) number K021447. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM?

TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2002-05-22. The listed applicant is Aerotel Medical Systems (1998) , Ltd.. The 510(k) number is K021447.

When did TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM receive FDA 510(k) clearance?

TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM received FDA 510(k) clearance on 2002-05-22, under 510(k) number K021447.

Who is the listed applicant for TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM?

The FDA 510(k) record lists Aerotel Medical Systems (1998) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM?

The FDA product code for TELE-CLINIQ DATA TRANSMISSION SYSTEM BLOOD PRESSURE MEASUREMENT SYSTEM is DXN.

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Other records listing Aerotel Medical Systems (1998) , Ltd. 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: DXN)

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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