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FDA 510(k)

SUN FILTERS/SHIELDS

K-Number: K941829 · 1994-05-17

Decision Date1994-05-17
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SUN FILTERS/SHIELDS is the device name listed in this FDA 510(k) record. The listed applicant is Klinger Eye Shields, Inc.. It received FDA 510(k) clearance on 1994-05-17 under 510(k) number K941829. 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 SUN FILTERS/SHIELDS?

SUN FILTERS/SHIELDS is a medical device that received FDA 510(k) clearance on 1994-05-17. The listed applicant is Klinger Eye Shields, Inc.. The 510(k) number is K941829.

When did SUN FILTERS/SHIELDS receive FDA 510(k) clearance?

SUN FILTERS/SHIELDS received FDA 510(k) clearance on 1994-05-17, under 510(k) number K941829.

Who is the listed applicant for SUN FILTERS/SHIELDS?

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

What is the FDA product code for SUN FILTERS/SHIELDS?

The FDA product code for SUN FILTERS/SHIELDS 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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