CLEEN-ABLE
K-Number: K994044 · 2000-02-25
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Device Summary
Frequently Asked Questions
What is the CLEEN-ABLE?
CLEEN-ABLE is a medical device that received FDA 510(k) clearance on 2000-02-25. The listed applicant is Vital Signs, Inc.. The 510(k) number is K994044.
When did CLEEN-ABLE receive FDA 510(k) clearance?
CLEEN-ABLE received FDA 510(k) clearance on 2000-02-25, under 510(k) number K994044.
Who is the listed applicant for CLEEN-ABLE?
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 CLEEN-ABLE?
The FDA product code for CLEEN-ABLE 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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