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FDA 510(k)

BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE

K-Number: K850893 · 1985-05-16

Decision Date1985-05-16
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE is the device name listed in this FDA 510(k) record. The listed applicant is Sun Dance Technology, Inc.. It received FDA 510(k) clearance on 1985-05-16 under 510(k) number K850893. 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/CLINIC SYS MEASUREMENT, BP NON-INVASIVE?

BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE is a medical device that received FDA 510(k) clearance on 1985-05-16. The listed applicant is Sun Dance Technology, Inc.. The 510(k) number is K850893.

When did BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE receive FDA 510(k) clearance?

BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE received FDA 510(k) clearance on 1985-05-16, under 510(k) number K850893.

Who is the listed applicant for BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE?

The FDA 510(k) record lists Sun Dance Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE?

The FDA product code for BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE 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.

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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