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FDA 510(k)

PANASONIC WRIST BLOOD PRESSURE METER

K-Number: K942422 · 1995-02-15

ApplicantKing & Spalding
Decision Date1995-02-15
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PANASONIC WRIST BLOOD PRESSURE METER is the device name listed in this FDA 510(k) record. The listed applicant is King & Spalding. It received FDA 510(k) clearance on 1995-02-15 under 510(k) number K942422. 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?

PANASONIC WRIST BLOOD PRESSURE METER is a medical device that received FDA 510(k) clearance on 1995-02-15. The listed applicant is King & Spalding. The 510(k) number is K942422.

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

PANASONIC WRIST BLOOD PRESSURE METER received FDA 510(k) clearance on 1995-02-15, under 510(k) number K942422.

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

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

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

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

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Other records listing King & Spalding 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.

K942423NAIS WRIST BLOOD PRESSURE METERK945998CHIN IMPLANT STYLE IK944408IMPLANTECH MEDICAL GRADE SILICONE SHEETINGK942420IMPLANTECH MIDFACE-SUBMALAR LE FORT IMPLANTK942421IMPLANTECH LATERAL MANDIBULAR BAR IMPLANTK941972HEMO-O-LOK

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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