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FDA 510(k)

PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284

K-Number: K981542 · 1999-03-03

Decision Date1999-03-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284 is the device name listed in this FDA 510(k) record. The listed applicant is Panasonic Corporation (Panasonic). It received FDA 510(k) clearance on 1999-03-03 under 510(k) number K981542. 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 PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284?

PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284 is a medical device that received FDA 510(k) clearance on 1999-03-03. The listed applicant is Panasonic Corporation (Panasonic). The 510(k) number is K981542.

When did PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284 receive FDA 510(k) clearance?

PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284 received FDA 510(k) clearance on 1999-03-03, under 510(k) number K981542.

Who is the listed applicant for PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284?

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

What is the FDA product code for PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284?

The FDA product code for PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284 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 Panasonic Corporation (Panasonic) 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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