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FDA 510(k)

BLOOD PRESSURE UNIT MODEL 410

K-Number: K802412 · 1980-12-16

ApplicantJs & A Group
Decision Date1980-12-16
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE UNIT MODEL 410 is the device name listed in this FDA 510(k) record. The listed applicant is Js & A Group. It received FDA 510(k) clearance on 1980-12-16 under 510(k) number K802412. 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 BLOOD PRESSURE UNIT MODEL 410?

BLOOD PRESSURE UNIT MODEL 410 is a medical device that received FDA 510(k) clearance on 1980-12-16. The listed applicant is Js & A Group. The 510(k) number is K802412.

When did BLOOD PRESSURE UNIT MODEL 410 receive FDA 510(k) clearance?

BLOOD PRESSURE UNIT MODEL 410 received FDA 510(k) clearance on 1980-12-16, under 510(k) number K802412.

Who is the listed applicant for BLOOD PRESSURE UNIT MODEL 410?

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

What is the FDA product code for BLOOD PRESSURE UNIT MODEL 410?

The FDA product code for BLOOD PRESSURE UNIT MODEL 410 is DXN.

Related Clinical Trials

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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Other records listing Js & A Group 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.

K802411BLOOD PRESSURE UNIT MODEL 310

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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