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FDA 510(k)

TL100 TENSMETER BLOOD PRESSURE MONITORING SYSTEM

K-Number: K022783 · 2002-11-19

Decision Date2002-11-19
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TL100 TENSMETER BLOOD PRESSURE MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Tensys Medical, Inc.. It received FDA 510(k) clearance on 2002-11-19 under 510(k) number K022783. 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 TL100 TENSMETER BLOOD PRESSURE MONITORING SYSTEM?

TL100 TENSMETER BLOOD PRESSURE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2002-11-19. The listed applicant is Tensys Medical, Inc.. The 510(k) number is K022783.

When did TL100 TENSMETER BLOOD PRESSURE MONITORING SYSTEM receive FDA 510(k) clearance?

TL100 TENSMETER BLOOD PRESSURE MONITORING SYSTEM received FDA 510(k) clearance on 2002-11-19, under 510(k) number K022783.

Who is the listed applicant for TL100 TENSMETER BLOOD PRESSURE MONITORING SYSTEM?

The FDA 510(k) record lists Tensys Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TL100 TENSMETER BLOOD PRESSURE MONITORING SYSTEM?

The FDA product code for TL100 TENSMETER BLOOD PRESSURE MONITORING SYSTEM is DXN.

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 Tensys Medical, Inc. 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: 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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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