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FDA 510(k)

HEALTHTEAM DIGITAL BLOOD PRESSURE KIT 8175

K-Number: K852459 · 1985-12-30

ApplicantHealthteam
Decision Date1985-12-30
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEALTHTEAM DIGITAL BLOOD PRESSURE KIT 8175 is the device name listed in this FDA 510(k) record. The listed applicant is Healthteam. It received FDA 510(k) clearance on 1985-12-30 under 510(k) number K852459. 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 HEALTHTEAM DIGITAL BLOOD PRESSURE KIT 8175?

HEALTHTEAM DIGITAL BLOOD PRESSURE KIT 8175 is a medical device that received FDA 510(k) clearance on 1985-12-30. The listed applicant is Healthteam. The 510(k) number is K852459.

When did HEALTHTEAM DIGITAL BLOOD PRESSURE KIT 8175 receive FDA 510(k) clearance?

HEALTHTEAM DIGITAL BLOOD PRESSURE KIT 8175 received FDA 510(k) clearance on 1985-12-30, under 510(k) number K852459.

Who is the listed applicant for HEALTHTEAM DIGITAL BLOOD PRESSURE KIT 8175?

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

What is the FDA product code for HEALTHTEAM DIGITAL BLOOD PRESSURE KIT 8175?

The FDA product code for HEALTHTEAM DIGITAL BLOOD PRESSURE KIT 8175 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.

Other records listing Healthteam 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.

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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.

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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