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FDA 510(k)

PANASONIC WRIST BLOOD PRESSURE MONITOR, MODELS EW 3031 AND EW 3032

K-Number: K033894 · 2004-03-11

ApplicantMatsushita Electric Works, Ltd.
Decision Date2004-03-11
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PANASONIC WRIST BLOOD PRESSURE MONITOR, MODELS EW 3031 AND EW 3032 is the device name listed in this FDA 510(k) record. The listed applicant is Matsushita Electric Works, Ltd.. It received FDA 510(k) clearance on 2004-03-11 under 510(k) number K033894. 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 MONITOR, MODELS EW 3031 AND EW 3032?

PANASONIC WRIST BLOOD PRESSURE MONITOR, MODELS EW 3031 AND EW 3032 is a medical device that received FDA 510(k) clearance on 2004-03-11. The listed applicant is Matsushita Electric Works, Ltd.. The 510(k) number is K033894.

When did PANASONIC WRIST BLOOD PRESSURE MONITOR, MODELS EW 3031 AND EW 3032 receive FDA 510(k) clearance?

PANASONIC WRIST BLOOD PRESSURE MONITOR, MODELS EW 3031 AND EW 3032 received FDA 510(k) clearance on 2004-03-11, under 510(k) number K033894.

Who is the listed applicant for PANASONIC WRIST BLOOD PRESSURE MONITOR, MODELS EW 3031 AND EW 3032?

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

What is the FDA product code for PANASONIC WRIST BLOOD PRESSURE MONITOR, MODELS EW 3031 AND EW 3032?

The FDA product code for PANASONIC WRIST BLOOD PRESSURE MONITOR, MODELS EW 3031 AND EW 3032 is DXN.

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Other records listing Matsushita Electric Works, 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.

K042818PANASONIC WRIST BLOOD PRESSURE MONITOR, MODELS EW3003 AND EW3037

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.

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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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