IV-TUBE SECURE
K-Number: K923882 · 1992-12-24
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Device Summary
Frequently Asked Questions
What is the IV-TUBE SECURE?
IV-TUBE SECURE is a medical device that received FDA 510(k) clearance on 1992-12-24. The listed applicant is Ximedix, Inc.. The 510(k) number is K923882.
When did IV-TUBE SECURE receive FDA 510(k) clearance?
IV-TUBE SECURE received FDA 510(k) clearance on 1992-12-24, under 510(k) number K923882.
Who is the listed applicant for IV-TUBE SECURE?
The FDA 510(k) record lists Ximedix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IV-TUBE SECURE?
The FDA product code for IV-TUBE SECURE is FPA.
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: FPA)
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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