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FDA 510(k)

DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1

K-Number: K881003 · 1988-05-18

ApplicantHealthcheck Corp.
Decision Date1988-05-18
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1 is the device name listed in this FDA 510(k) record. The listed applicant is Healthcheck Corp.. It received FDA 510(k) clearance on 1988-05-18 under 510(k) number K881003. 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 DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1?

DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1 is a medical device that received FDA 510(k) clearance on 1988-05-18. The listed applicant is Healthcheck Corp.. The 510(k) number is K881003.

When did DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1 receive FDA 510(k) clearance?

DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1 received FDA 510(k) clearance on 1988-05-18, under 510(k) number K881003.

Who is the listed applicant for DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1?

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

What is the FDA product code for DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1?

The FDA product code for DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1 is DXN.

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Other records listing Healthcheck Corp. 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.

K884489C&T PREGNANCY TEST KITK874818TENSTARK863181HEALTHCHECK THERM-STRIPK861946PTK PLUS. HOME PREGNANCY TESTK860287PULSONIC DIGITAL BLOOD PRESSURE MONITOR MODEL BP-3K851379HEALTHCHECK DIGITAL THERMOMETER MODEL 1 TH-2

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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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