UNITY DISPOSABLE INCONTINENT BRIEF
K-Number: K860459 · 1986-02-26
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Device Summary
Frequently Asked Questions
What is the UNITY DISPOSABLE INCONTINENT BRIEF?
UNITY DISPOSABLE INCONTINENT BRIEF is a medical device that received FDA 510(k) clearance on 1986-02-26. The listed applicant is Bevan Medical, Inc.. The 510(k) number is K860459.
When did UNITY DISPOSABLE INCONTINENT BRIEF receive FDA 510(k) clearance?
UNITY DISPOSABLE INCONTINENT BRIEF received FDA 510(k) clearance on 1986-02-26, under 510(k) number K860459.
Who is the listed applicant for UNITY DISPOSABLE INCONTINENT BRIEF?
The FDA 510(k) record lists Bevan Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNITY DISPOSABLE INCONTINENT BRIEF?
The FDA product code for UNITY DISPOSABLE INCONTINENT BRIEF is EYQ.
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 Bevan 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: EYQ)
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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