CLEVER TD-3018A BLOOD PRESSURE MONITOR
K-Number: K051703 · 2005-08-12
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Device Summary
Frequently Asked Questions
What is the CLEVER TD-3018A BLOOD PRESSURE MONITOR?
CLEVER TD-3018A BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 2005-08-12. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K051703.
When did CLEVER TD-3018A BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?
CLEVER TD-3018A BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 2005-08-12, under 510(k) number K051703.
Who is the listed applicant for CLEVER TD-3018A BLOOD PRESSURE MONITOR?
The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLEVER TD-3018A BLOOD PRESSURE MONITOR?
The FDA product code for CLEVER TD-3018A BLOOD PRESSURE MONITOR 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 Taidoc Technology Corporation 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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