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FDA 510(k)

MICRONTA BP-1 ELECTRONIC B/P TESTER

K-Number: K800225 · 1980-03-10

ApplicantTandy Corp.
Decision Date1980-03-10
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRONTA BP-1 ELECTRONIC B/P TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Tandy Corp.. It received FDA 510(k) clearance on 1980-03-10 under 510(k) number K800225. 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 MICRONTA BP-1 ELECTRONIC B/P TESTER?

MICRONTA BP-1 ELECTRONIC B/P TESTER is a medical device that received FDA 510(k) clearance on 1980-03-10. The listed applicant is Tandy Corp.. The 510(k) number is K800225.

When did MICRONTA BP-1 ELECTRONIC B/P TESTER receive FDA 510(k) clearance?

MICRONTA BP-1 ELECTRONIC B/P TESTER received FDA 510(k) clearance on 1980-03-10, under 510(k) number K800225.

Who is the listed applicant for MICRONTA BP-1 ELECTRONIC B/P TESTER?

The FDA 510(k) record lists Tandy Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRONTA BP-1 ELECTRONIC B/P TESTER?

The FDA product code for MICRONTA BP-1 ELECTRONIC B/P TESTER 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.

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.

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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