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FDA 510(k)

FORTEC MI-100, MI-50 DIGITAL BLOOD PRESSURE METER

K-Number: K873765 · 1987-10-09

Decision Date1987-10-09
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FORTEC MI-100, MI-50 DIGITAL BLOOD PRESSURE METER is the device name listed in this FDA 510(k) record. The listed applicant is Nam Tai , Ltd.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K873765. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORTEC MI-100, MI-50 DIGITAL BLOOD PRESSURE METER?

FORTEC MI-100, MI-50 DIGITAL BLOOD PRESSURE METER is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Nam Tai , Ltd.. The 510(k) number is K873765.

When did FORTEC MI-100, MI-50 DIGITAL BLOOD PRESSURE METER receive FDA 510(k) clearance?

FORTEC MI-100, MI-50 DIGITAL BLOOD PRESSURE METER received FDA 510(k) clearance on 1987-10-09, under 510(k) number K873765.

Who is the listed applicant for FORTEC MI-100, MI-50 DIGITAL BLOOD PRESSURE METER?

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

What is the FDA product code for FORTEC MI-100, MI-50 DIGITAL BLOOD PRESSURE METER?

The FDA product code for FORTEC MI-100, MI-50 DIGITAL BLOOD PRESSURE METER is DSK.

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.

Other records listing Nam Tai , Ltd. 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.

Related Devices (Code: DSK)

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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