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FDA 510(k)

IV SECUREMENT DEVICE USING HYTREL THERMO. FILM

K-Number: K870090 · 1987-02-04

ApplicantAvery Intl.
Decision Date1987-02-04
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IV SECUREMENT DEVICE USING HYTREL THERMO. FILM is the device name listed in this FDA 510(k) record. The listed applicant is Avery Intl.. It received FDA 510(k) clearance on 1987-02-04 under 510(k) number K870090. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IV SECUREMENT DEVICE USING HYTREL THERMO. FILM?

IV SECUREMENT DEVICE USING HYTREL THERMO. FILM 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 K870090.

When did IV SECUREMENT DEVICE USING HYTREL THERMO. FILM receive FDA 510(k) clearance?

IV SECUREMENT DEVICE USING HYTREL THERMO. FILM received FDA 510(k) clearance on 1987-02-04, under 510(k) number K870090.

Who is the listed applicant for IV SECUREMENT DEVICE USING HYTREL THERMO. FILM?

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 USING HYTREL THERMO. FILM?

The FDA product code for IV SECUREMENT DEVICE USING HYTREL THERMO. FILM 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.

View all 12 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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