AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100
K-Number: K994423 · 2000-03-28
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Device Summary
Frequently Asked Questions
What is the AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100?
AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100 is a medical device that received FDA 510(k) clearance on 2000-03-28. The listed applicant is Vsm Medtech , Ltd.. The 510(k) number is K994423.
When did AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100 receive FDA 510(k) clearance?
AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100 received FDA 510(k) clearance on 2000-03-28, under 510(k) number K994423.
Who is the listed applicant for AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100?
The FDA 510(k) record lists Vsm Medtech , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100?
The FDA product code for AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100 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 Vsm Medtech , 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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