IV SECUREMENT DEVICE
K-Number: K870020 · 1987-02-04
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Device Summary
Frequently Asked Questions
What is the IV SECUREMENT DEVICE?
IV SECUREMENT DEVICE is a medical device that received FDA 510(k) clearance on 1987-02-04. The listed applicant is Avery Intl.. The 510(k) number is K870020.
When did IV SECUREMENT DEVICE receive FDA 510(k) clearance?
IV SECUREMENT DEVICE received FDA 510(k) clearance on 1987-02-04, under 510(k) number K870020.
Who is the listed applicant for IV SECUREMENT DEVICE?
The FDA 510(k) record lists Avery Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IV SECUREMENT DEVICE?
The FDA product code for IV SECUREMENT DEVICE is KGX.
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 Avery Intl. 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: KGX)
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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