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FDA 510(k)

HEALTHPAK UTILITY SOX BARRIERS

K-Number: K923306 · 1992-08-05

Decision Date1992-08-05
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HEALTHPAK UTILITY SOX BARRIERS is the device name listed in this FDA 510(k) record. The listed applicant is Healthpak, Inc.. It received FDA 510(k) clearance on 1992-08-05 under 510(k) number K923306. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEALTHPAK UTILITY SOX BARRIERS?

HEALTHPAK UTILITY SOX BARRIERS is a medical device that received FDA 510(k) clearance on 1992-08-05. The listed applicant is Healthpak, Inc.. The 510(k) number is K923306.

When did HEALTHPAK UTILITY SOX BARRIERS receive FDA 510(k) clearance?

HEALTHPAK UTILITY SOX BARRIERS received FDA 510(k) clearance on 1992-08-05, under 510(k) number K923306.

Who is the listed applicant for HEALTHPAK UTILITY SOX BARRIERS?

The FDA 510(k) record lists Healthpak, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEALTHPAK UTILITY SOX BARRIERS?

The FDA product code for HEALTHPAK UTILITY SOX BARRIERS is KLC.

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 Healthpak, Inc. 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: KLC)

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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