POLYURETHANE BLOOD PRESSURE CUFFS
K-Number: K041689 · 2004-08-06
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Device Summary
Frequently Asked Questions
What is the POLYURETHANE BLOOD PRESSURE CUFFS?
POLYURETHANE BLOOD PRESSURE CUFFS is a medical device that received FDA 510(k) clearance on 2004-08-06. The listed applicant is D. E. Hokanson, Inc.. The 510(k) number is K041689.
When did POLYURETHANE BLOOD PRESSURE CUFFS receive FDA 510(k) clearance?
POLYURETHANE BLOOD PRESSURE CUFFS received FDA 510(k) clearance on 2004-08-06, under 510(k) number K041689.
Who is the listed applicant for POLYURETHANE BLOOD PRESSURE CUFFS?
The FDA 510(k) record lists D. E. Hokanson, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POLYURETHANE BLOOD PRESSURE CUFFS?
The FDA product code for POLYURETHANE 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 D. E. Hokanson, 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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