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FDA 510(k)

LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)

K-Number: K930198 · 1993-08-23

ApplicantForda (China) Optical Co.
Decision Date1993-08-23
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) is the device name listed in this FDA 510(k) record. The listed applicant is Forda (China) Optical Co.. It received FDA 510(k) clearance on 1993-08-23 under 510(k) number K930198. 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 LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)?

LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) is a medical device that received FDA 510(k) clearance on 1993-08-23. The listed applicant is Forda (China) Optical Co.. The 510(k) number is K930198.

When did LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) receive FDA 510(k) clearance?

LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) received FDA 510(k) clearance on 1993-08-23, under 510(k) number K930198.

Who is the listed applicant for LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)?

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

What is the FDA product code for LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)?

The FDA product code for LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) is HQY.

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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.

K974852NON-PRESCRIPTION SUNGLASSESChia Hui Spectacles Mfg. Corp.K974860NON-PRESCRIPTION SUNGLASSESWenzhou Ming Ming Optical Co. , Ltd.K974861NON-PRESCRIPTION SUNGLASSESWenzhou Hindar Optical Co., Ltd.K974511SUNGLASSESSun World Intl., Inc.K974441SUNGLASSESHip Shing Fat Co., Ltd.K973528SUNGLASSESJeou Jeou Long Industrial Co., Ltd.

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.

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