TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM
K-Number: K020537 · 2002-08-15
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Device Summary
Frequently Asked Questions
What is the TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM?
TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2002-08-15. The listed applicant is Tensys Medical, Inc.. The 510(k) number is K020537.
When did TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM receive FDA 510(k) clearance?
TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM received FDA 510(k) clearance on 2002-08-15, under 510(k) number K020537.
Who is the listed applicant for TL10 TENSYMETER 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 TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM?
The FDA product code for TL10 TENSYMETER 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
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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