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FDA 510(k)

ACTION MEDTEK FACE SHIELD

K-Number: K926438 · 1993-08-18

Decision Date1993-08-18
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ACTION MEDTEK FACE SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Action Eyewear Corp.. It received FDA 510(k) clearance on 1993-08-18 under 510(k) number K926438. The device is classified under product code LYU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTION MEDTEK FACE SHIELD?

ACTION MEDTEK FACE SHIELD is a medical device that received FDA 510(k) clearance on 1993-08-18. The listed applicant is Action Eyewear Corp.. The 510(k) number is K926438.

When did ACTION MEDTEK FACE SHIELD receive FDA 510(k) clearance?

ACTION MEDTEK FACE SHIELD received FDA 510(k) clearance on 1993-08-18, under 510(k) number K926438.

Who is the listed applicant for ACTION MEDTEK FACE SHIELD?

The FDA 510(k) record lists Action Eyewear Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACTION MEDTEK FACE SHIELD?

The FDA product code for ACTION MEDTEK FACE SHIELD is LYU.

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 Action Eyewear Corp. 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: LYU)

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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