FOOTHILLS SURGICAL DRAPES
K-Number: K041224 · 2005-02-03
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Device Summary
Frequently Asked Questions
What is the FOOTHILLS SURGICAL DRAPES?
FOOTHILLS SURGICAL DRAPES is a medical device that received FDA 510(k) clearance on 2005-02-03. The listed applicant is Foothills Industries, Inc.. The 510(k) number is K041224.
When did FOOTHILLS SURGICAL DRAPES receive FDA 510(k) clearance?
FOOTHILLS SURGICAL DRAPES received FDA 510(k) clearance on 2005-02-03, under 510(k) number K041224.
Who is the listed applicant for FOOTHILLS SURGICAL DRAPES?
The FDA 510(k) record lists Foothills Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FOOTHILLS SURGICAL DRAPES?
The FDA product code for FOOTHILLS SURGICAL DRAPES is KKX.
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.
Related Devices (Code: KKX)
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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