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FDA 510(k)

MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER

K-Number: K872144 · 1987-07-29

Decision Date1987-07-29
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER is the device name listed in this FDA 510(k) record. The listed applicant is Vestra-Subco, Inc.. It received FDA 510(k) clearance on 1987-07-29 under 510(k) number K872144. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER?

MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER is a medical device that received FDA 510(k) clearance on 1987-07-29. The listed applicant is Vestra-Subco, Inc.. The 510(k) number is K872144.

When did MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER receive FDA 510(k) clearance?

MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER received FDA 510(k) clearance on 1987-07-29, under 510(k) number K872144.

Who is the listed applicant for MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER?

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

What is the FDA product code for MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER?

The FDA product code for MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER is DXQ.

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: DXQ)

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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