Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SPECTACLE FRAME/EYEGLASS FRAME

K-Number: K935558 · 1994-01-25

Decision Date1994-01-25
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE FRAME/EYEGLASS FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Modern Optical , Ltd.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K935558. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECTACLE FRAME/EYEGLASS FRAME?

SPECTACLE FRAME/EYEGLASS FRAME is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Modern Optical , Ltd.. The 510(k) number is K935558.

When did SPECTACLE FRAME/EYEGLASS FRAME receive FDA 510(k) clearance?

SPECTACLE FRAME/EYEGLASS FRAME received FDA 510(k) clearance on 1994-01-25, under 510(k) number K935558.

Who is the listed applicant for SPECTACLE FRAME/EYEGLASS FRAME?

The FDA 510(k) record lists Modern Optical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTACLE FRAME/EYEGLASS FRAME?

The FDA product code for SPECTACLE FRAME/EYEGLASS FRAME is HQZ.

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: HQZ)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑