FORTEC MI-150 DIGITAL BLOOD PRESSURE METER
K-Number: K884405 · 1989-05-19
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Device Summary
Frequently Asked Questions
What is the FORTEC MI-150 DIGITAL BLOOD PRESSURE METER?
FORTEC MI-150 DIGITAL BLOOD PRESSURE METER is a medical device that received FDA 510(k) clearance on 1989-05-19. The listed applicant is Nam Tai Electronic & Electrical Products, Ltd.. The 510(k) number is K884405.
When did FORTEC MI-150 DIGITAL BLOOD PRESSURE METER receive FDA 510(k) clearance?
FORTEC MI-150 DIGITAL BLOOD PRESSURE METER received FDA 510(k) clearance on 1989-05-19, under 510(k) number K884405.
Who is the listed applicant for FORTEC MI-150 DIGITAL BLOOD PRESSURE METER?
The FDA 510(k) record lists Nam Tai Electronic & Electrical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORTEC MI-150 DIGITAL BLOOD PRESSURE METER?
The FDA product code for FORTEC MI-150 DIGITAL BLOOD PRESSURE METER 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.
Other records listing Nam Tai Electronic & Electrical Products, 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: 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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