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FDA 510(k)

NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T

K-Number: K041789 · 2004-07-15

Decision Date2004-07-15
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T is the device name listed in this FDA 510(k) record. The listed applicant is Meditec Co., Ltd.. It received FDA 510(k) clearance on 2004-07-15 under 510(k) number K041789. 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 NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T?

NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T is a medical device that received FDA 510(k) clearance on 2004-07-15. The listed applicant is Meditec Co., Ltd.. The 510(k) number is K041789.

When did NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T receive FDA 510(k) clearance?

NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T received FDA 510(k) clearance on 2004-07-15, under 510(k) number K041789.

Who is the listed applicant for NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T?

The FDA 510(k) record lists Meditec Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T?

The FDA product code for NONINVASIVE BLOOD PRESSURE MONITOR, MODELS MD-880B AND MD-900T 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 Meditec Co., 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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