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FDA 510(k)

IV SECUREMENT DEVICES

K-Number: K854464 · 1986-03-03

ApplicantAvery Intl.
Decision Date1986-03-03
Product CodeFRO
DecisionSubstantially Equivalent for Some Indications

Device Summary

IV SECUREMENT DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Avery Intl.. It received FDA 510(k) clearance on 1986-03-03 under 510(k) number K854464. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the IV SECUREMENT DEVICES?

IV SECUREMENT DEVICES is a medical device that received FDA 510(k) clearance on 1986-03-03. The listed applicant is Avery Intl.. The 510(k) number is K854464.

When did IV SECUREMENT DEVICES receive FDA 510(k) clearance?

IV SECUREMENT DEVICES received FDA 510(k) clearance on 1986-03-03, under 510(k) number K854464.

Who is the listed applicant for IV SECUREMENT DEVICES?

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 DEVICES?

The FDA product code for IV SECUREMENT DEVICES is FRO. This falls under the Anesthesiology category.

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.

View all 12 devices →

Related Devices (Code: FRO)

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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