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FDA 510(k)

KASEY EYE SHIELD

K-Number: K863474 · 1986-09-24

Decision Date1986-09-24
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KASEY EYE SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Kasey Enterprises, Inc.. It received FDA 510(k) clearance on 1986-09-24 under 510(k) number K863474. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KASEY EYE SHIELD?

KASEY EYE SHIELD is a medical device that received FDA 510(k) clearance on 1986-09-24. The listed applicant is Kasey Enterprises, Inc.. The 510(k) number is K863474.

When did KASEY EYE SHIELD receive FDA 510(k) clearance?

KASEY EYE SHIELD received FDA 510(k) clearance on 1986-09-24, under 510(k) number K863474.

Who is the listed applicant for KASEY EYE SHIELD?

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

What is the FDA product code for KASEY EYE SHIELD?

The FDA product code for KASEY EYE SHIELD is HOY.

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.

Related Devices (Code: HOY)

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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