TL-300 T-LINE NON-INVASIVE BLOOD PRESSURE MONITORING SYSTEM
K-Number: K123446 · 2012-12-07
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Device Summary
Frequently Asked Questions
What is the TL-300 T-LINE NON-INVASIVE BLOOD PRESSURE MONITORING SYSTEM?
TL-300 T-LINE NON-INVASIVE BLOOD PRESSURE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2012-12-07. The listed applicant is United States Gtm Medical Devices, Inc.. The 510(k) number is K123446.
When did TL-300 T-LINE NON-INVASIVE BLOOD PRESSURE MONITORING SYSTEM receive FDA 510(k) clearance?
TL-300 T-LINE NON-INVASIVE BLOOD PRESSURE MONITORING SYSTEM received FDA 510(k) clearance on 2012-12-07, under 510(k) number K123446.
Who is the listed applicant for TL-300 T-LINE NON-INVASIVE BLOOD PRESSURE MONITORING SYSTEM?
The FDA 510(k) record lists United States Gtm Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TL-300 T-LINE NON-INVASIVE BLOOD PRESSURE MONITORING SYSTEM?
The FDA product code for TL-300 T-LINE NON-INVASIVE 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.
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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