BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF
K-Number: K912007 · 1991-07-22
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Device Summary
Frequently Asked Questions
What is the BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF?
BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 1991-07-22. The listed applicant is Tecnadyne Scientific, Inc.. The 510(k) number is K912007.
When did BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF receive FDA 510(k) clearance?
BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF received FDA 510(k) clearance on 1991-07-22, under 510(k) number K912007.
Who is the listed applicant for BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF?
The FDA 510(k) record lists Tecnadyne Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF?
The FDA product code for BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF 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 Tecnadyne Scientific, 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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