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FDA 510(k)

CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER

K-Number: K954547 · 1997-04-01

ApplicantCitizen Watch Co., Ltd.
Decision Date1997-04-01
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Citizen Watch Co., Ltd.. It received FDA 510(k) clearance on 1997-04-01 under 510(k) number K954547. 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 CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER?

CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1997-04-01. The listed applicant is Citizen Watch Co., Ltd.. The 510(k) number is K954547.

When did CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER receive FDA 510(k) clearance?

CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER received FDA 510(k) clearance on 1997-04-01, under 510(k) number K954547.

Who is the listed applicant for CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER?

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

What is the FDA product code for CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER?

The FDA product code for CH-502A & CH520B DIGITAL FINGER SPHYGMOMANOMETER is DXN.

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Other records listing Citizen Watch 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.

K061161BLOOD PRESSURE METER, MODEL CH-311BK052046BLOOD PRESSURE METER, MODEL CH-432K001244BLOOD PRESSURE METER, MODELS CH-631B, CH-631D, CH-632B, CH-632DK984223BLOOD PRESSURE METER, MODELS CH-491, CH-481, CH-471K973061CH-601A AND CH-601B DIGITAL WRIST SPHYGMOMANOMETER (CH-601A/CH-601B)K923344ELECTRONIC DIGITAL BLOOD PRESSURE MONITOR

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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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