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FDA 510(k)

BP 5000

K-Number: K843137 · 1985-01-16

ApplicantTech Vend Marketing
Decision Date1985-01-16
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BP 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Tech Vend Marketing. It received FDA 510(k) clearance on 1985-01-16 under 510(k) number K843137. 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 BP 5000?

BP 5000 is a medical device that received FDA 510(k) clearance on 1985-01-16. The listed applicant is Tech Vend Marketing. The 510(k) number is K843137.

When did BP 5000 receive FDA 510(k) clearance?

BP 5000 received FDA 510(k) clearance on 1985-01-16, under 510(k) number K843137.

Who is the listed applicant for BP 5000?

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

What is the FDA product code for BP 5000?

The FDA product code for BP 5000 is DXN.

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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