BLOOD PRESSURE CUFFS
K-Number: K912638 · 1991-07-25
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Device Summary
Frequently Asked Questions
What is the BLOOD PRESSURE CUFFS?
BLOOD PRESSURE CUFFS is a medical device that received FDA 510(k) clearance on 1991-07-25. The listed applicant is Vital Signs, Inc.. The 510(k) number is K912638.
When did BLOOD PRESSURE CUFFS receive FDA 510(k) clearance?
BLOOD PRESSURE CUFFS received FDA 510(k) clearance on 1991-07-25, under 510(k) number K912638.
Who is the listed applicant for BLOOD PRESSURE CUFFS?
The FDA 510(k) record lists Vital Signs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD PRESSURE CUFFS?
The FDA product code for BLOOD PRESSURE CUFFS 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.
Other records listing Vital Signs, Inc. 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: 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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