MICRONTA BP-1 ELECTRONIC B/P TESTER
K-Number: K800225 · 1980-03-10
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Device Summary
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
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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