TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII
K-Number: K011058 · 2001-10-23
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Device Summary
Frequently Asked Questions
What is the TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII?
TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII is a medical device that received FDA 510(k) clearance on 2001-10-23. The listed applicant is Meridian Medical Technologies , Ltd.. The 510(k) number is K011058.
When did TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII receive FDA 510(k) clearance?
TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII received FDA 510(k) clearance on 2001-10-23, under 510(k) number K011058.
Who is the listed applicant for TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII?
The FDA 510(k) record lists Meridian Medical Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII?
The FDA product code for TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII 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 Meridian Medical Technologies , 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.
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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