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FDA 510(k)

ANEROID SPHYGMOMANOMETERS/MERCURIAL SPHYGMOMANOMETERSRS

K-Number: K942543 · 1995-07-14

ApplicantSankei Co., Ltd.
Decision Date1995-07-14
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANEROID SPHYGMOMANOMETERS/MERCURIAL SPHYGMOMANOMETERSRS is the device name listed in this FDA 510(k) record. The listed applicant is Sankei Co., Ltd.. It received FDA 510(k) clearance on 1995-07-14 under 510(k) number K942543. 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 ANEROID SPHYGMOMANOMETERS/MERCURIAL SPHYGMOMANOMETERSRS?

ANEROID SPHYGMOMANOMETERS/MERCURIAL SPHYGMOMANOMETERSRS is a medical device that received FDA 510(k) clearance on 1995-07-14. The listed applicant is Sankei Co., Ltd.. The 510(k) number is K942543.

When did ANEROID SPHYGMOMANOMETERS/MERCURIAL SPHYGMOMANOMETERSRS receive FDA 510(k) clearance?

ANEROID SPHYGMOMANOMETERS/MERCURIAL SPHYGMOMANOMETERSRS received FDA 510(k) clearance on 1995-07-14, under 510(k) number K942543.

Who is the listed applicant for ANEROID SPHYGMOMANOMETERS/MERCURIAL SPHYGMOMANOMETERSRS?

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

What is the FDA product code for ANEROID SPHYGMOMANOMETERS/MERCURIAL SPHYGMOMANOMETERSRS?

The FDA product code for ANEROID SPHYGMOMANOMETERS/MERCURIAL SPHYGMOMANOMETERSRS is DXN.

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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.

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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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