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FDA 510(k)

NON-INVASIVE BLOOD PRESSURE MODULE

K-Number: K894945 · 1989-10-26

ApplicantMarquette Electronics, Inc.
Decision Date1989-10-26
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NON-INVASIVE BLOOD PRESSURE MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Electronics, Inc.. It received FDA 510(k) clearance on 1989-10-26 under 510(k) number K894945. 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 NON-INVASIVE BLOOD PRESSURE MODULE?

NON-INVASIVE BLOOD PRESSURE MODULE is a medical device that received FDA 510(k) clearance on 1989-10-26. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K894945.

When did NON-INVASIVE BLOOD PRESSURE MODULE receive FDA 510(k) clearance?

NON-INVASIVE BLOOD PRESSURE MODULE received FDA 510(k) clearance on 1989-10-26, under 510(k) number K894945.

Who is the listed applicant for NON-INVASIVE BLOOD PRESSURE MODULE?

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

What is the FDA product code for NON-INVASIVE BLOOD PRESSURE MODULE?

The FDA product code for NON-INVASIVE BLOOD PRESSURE MODULE is DXN.

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Other records listing Marquette Electronics, Inc. as applicant

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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