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FDA 510(k)

WRIST BLOOD PRESSURE METER MODEL SE-330

K-Number: K973078 · 1999-05-20

Decision Date1999-05-20
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WRIST BLOOD PRESSURE METER MODEL SE-330 is the device name listed in this FDA 510(k) record. The listed applicant is Sein Electronics Co., Ltd.. It received FDA 510(k) clearance on 1999-05-20 under 510(k) number K973078. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRIST BLOOD PRESSURE METER MODEL SE-330?

WRIST BLOOD PRESSURE METER MODEL SE-330 is a medical device that received FDA 510(k) clearance on 1999-05-20. The listed applicant is Sein Electronics Co., Ltd.. The 510(k) number is K973078.

When did WRIST BLOOD PRESSURE METER MODEL SE-330 receive FDA 510(k) clearance?

WRIST BLOOD PRESSURE METER MODEL SE-330 received FDA 510(k) clearance on 1999-05-20, under 510(k) number K973078.

Who is the listed applicant for WRIST BLOOD PRESSURE METER MODEL SE-330?

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

What is the FDA product code for WRIST BLOOD PRESSURE METER MODEL SE-330?

The FDA product code for WRIST BLOOD PRESSURE METER MODEL SE-330 is DPW.

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 Sein Electronics 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.

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Related Devices (Code: DPW)

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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