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FDA 510(k)

SPECTACLE FRAMES (WING SHING OPTICAL)

K-Number: K940077 · 1994-04-12

Decision Date1994-04-12
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE FRAMES (WING SHING OPTICAL) is the device name listed in this FDA 510(k) record. The listed applicant is Continental Optical Imports. It received FDA 510(k) clearance on 1994-04-12 under 510(k) number K940077. 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 FRAMES (WING SHING OPTICAL)?

SPECTACLE FRAMES (WING SHING OPTICAL) is a medical device that received FDA 510(k) clearance on 1994-04-12. The listed applicant is Continental Optical Imports. The 510(k) number is K940077.

When did SPECTACLE FRAMES (WING SHING OPTICAL) receive FDA 510(k) clearance?

SPECTACLE FRAMES (WING SHING OPTICAL) received FDA 510(k) clearance on 1994-04-12, under 510(k) number K940077.

Who is the listed applicant for SPECTACLE FRAMES (WING SHING OPTICAL)?

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

What is the FDA product code for SPECTACLE FRAMES (WING SHING OPTICAL)?

The FDA product code for SPECTACLE FRAMES (WING SHING OPTICAL) 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.

Other records listing Continental Optical Imports 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: 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

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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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