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FDA 510(k)

YKI-770 ELECTRONIC SPHYGMOMAMETER

K-Number: K842318 · 1985-02-14

ApplicantYukosha Co., Inc.
Decision Date1985-02-14
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

YKI-770 ELECTRONIC SPHYGMOMAMETER is the device name listed in this FDA 510(k) record. The listed applicant is Yukosha Co., Inc.. It received FDA 510(k) clearance on 1985-02-14 under 510(k) number K842318. 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 YKI-770 ELECTRONIC SPHYGMOMAMETER?

YKI-770 ELECTRONIC SPHYGMOMAMETER is a medical device that received FDA 510(k) clearance on 1985-02-14. The listed applicant is Yukosha Co., Inc.. The 510(k) number is K842318.

When did YKI-770 ELECTRONIC SPHYGMOMAMETER receive FDA 510(k) clearance?

YKI-770 ELECTRONIC SPHYGMOMAMETER received FDA 510(k) clearance on 1985-02-14, under 510(k) number K842318.

Who is the listed applicant for YKI-770 ELECTRONIC SPHYGMOMAMETER?

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

What is the FDA product code for YKI-770 ELECTRONIC SPHYGMOMAMETER?

The FDA product code for YKI-770 ELECTRONIC SPHYGMOMAMETER 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 Yukosha Co., Inc. 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.

K842317SIGNAL ELECTRONIC CLINICAL THERMOMETER

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.

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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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