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FDA 510(k)

AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100

K-Number: K994423 · 2000-03-28

Decision Date2000-03-28
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100 is the device name listed in this FDA 510(k) record. The listed applicant is Vsm Medtech , Ltd.. It received FDA 510(k) clearance on 2000-03-28 under 510(k) number K994423. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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