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FDA 510(k)

BLOOD-PRESSURE METER, BPW120

K-Number: K050083 · 2005-04-08

Decision Date2005-04-08
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD-PRESSURE METER, BPW120 is the device name listed in this FDA 510(k) record. The listed applicant is Idt Technology Limited. It received FDA 510(k) clearance on 2005-04-08 under 510(k) number K050083. 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 BLOOD-PRESSURE METER, BPW120?

BLOOD-PRESSURE METER, BPW120 is a medical device that received FDA 510(k) clearance on 2005-04-08. The listed applicant is Idt Technology Limited. The 510(k) number is K050083.

When did BLOOD-PRESSURE METER, BPW120 receive FDA 510(k) clearance?

BLOOD-PRESSURE METER, BPW120 received FDA 510(k) clearance on 2005-04-08, under 510(k) number K050083.

Who is the listed applicant for BLOOD-PRESSURE METER, BPW120?

The FDA 510(k) record lists Idt Technology Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD-PRESSURE METER, BPW120?

The FDA product code for BLOOD-PRESSURE METER, BPW120 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 Idt Technology Limited 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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