MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER
K-Number: K872144 · 1987-07-29
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Device Summary
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
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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