DEVON ACCUBP CUFF
K-Number: K090664 · 2009-03-23
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Device Summary
Frequently Asked Questions
What is the DEVON ACCUBP CUFF?
DEVON ACCUBP CUFF is a medical device that received FDA 510(k) clearance on 2009-03-23. The listed applicant is Devon Medical, Inc.. The 510(k) number is K090664.
When did DEVON ACCUBP CUFF receive FDA 510(k) clearance?
DEVON ACCUBP CUFF received FDA 510(k) clearance on 2009-03-23, under 510(k) number K090664.
Who is the listed applicant for DEVON ACCUBP CUFF?
The FDA 510(k) record lists Devon Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEVON ACCUBP CUFF?
The FDA product code for DEVON ACCUBP 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 Devon Medical, 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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