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FDA 510(k)

PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW280

K-Number: K981431 · 1999-03-03

ApplicantPanasonic Corporation (Panasonic)
Decision Date1999-03-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW280 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 K981431. 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 EW280?

PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW280 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 K981431.

When did PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW280 receive FDA 510(k) clearance?

PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW280 received FDA 510(k) clearance on 1999-03-03, under 510(k) number K981431.

Who is the listed applicant for PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW280?

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 EW280?

The FDA product code for PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW280 is DXN.

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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.

K981542PANASONIC WRIST BLOOD PRESSURE METER, MODEL EW284

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.

K261929Upper Arm Blood pressure monitor (BP7155D)OMRON Healthcare, Inc.K254000Happy Health Blood Pressure MonitorHappy Health, Inc.K262658Automatic Digital Blood Pressure monitor (LD-526)Honsun (Nantong) Co., Ltd.K261394Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus, DBP-61E3 Plus, DBP-61E2 Plus, DBP-62E3B Plus, DBP-62E2B Plus)JOYTECH Healthcare Co., Ltd.K253425Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6194-P,DBP-6294B-P,DBP-6195P,DBP-6295B-P, DBP-6196P,DBP-6296B-P,DBP-61E1-P, DBP-62E1B-P,DBP-62E3B-P,DBP-61E2-P,DBP-62E2B-P,DBP-61E3-P,DBP-6173-P,DBP-6273B-P,DBP-6179-P,DBP-6279B-P)Joytech Healthcare Co. , Ltd.K261061BP Go (BPP-855)Wellvii, Inc.

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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