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FDA 510(k)

NEW EYES EYEGLASS FRAME

K-Number: K940250 · 1994-04-19

Decision Date1994-04-19
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NEW EYES EYEGLASS FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise International Business. It received FDA 510(k) clearance on 1994-04-19 under 510(k) number K940250. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW EYES EYEGLASS FRAME?

NEW EYES EYEGLASS FRAME is a medical device that received FDA 510(k) clearance on 1994-04-19. The listed applicant is Sunrise International Business. The 510(k) number is K940250.

When did NEW EYES EYEGLASS FRAME receive FDA 510(k) clearance?

NEW EYES EYEGLASS FRAME received FDA 510(k) clearance on 1994-04-19, under 510(k) number K940250.

Who is the listed applicant for NEW EYES EYEGLASS FRAME?

The FDA 510(k) record lists Sunrise International Business as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEW EYES EYEGLASS FRAME?

The FDA product code for NEW EYES EYEGLASS FRAME is HQY.

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: HQY)

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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