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FDA 510(k)

HEALTHPAK X-RAY SOX BARRIERS

K-Number: K923307 · 1993-01-21

Decision Date1993-01-21
Product CodeEAP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HEALTHPAK X-RAY 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 1993-01-21 under 510(k) number K923307. The device is classified under product code EAP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEALTHPAK X-RAY SOX BARRIERS?

HEALTHPAK X-RAY SOX BARRIERS is a medical device that received FDA 510(k) clearance on 1993-01-21. The listed applicant is Healthpak, Inc.. The 510(k) number is K923307.

When did HEALTHPAK X-RAY SOX BARRIERS receive FDA 510(k) clearance?

HEALTHPAK X-RAY SOX BARRIERS received FDA 510(k) clearance on 1993-01-21, under 510(k) number K923307.

Who is the listed applicant for HEALTHPAK X-RAY 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 X-RAY SOX BARRIERS?

The FDA product code for HEALTHPAK X-RAY SOX BARRIERS is EAP.

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: EAP)

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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