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FDA 510(k)

MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS

K-Number: K900520 · 1990-05-03

ApplicantJ & B Assoc.
Decision Date1990-05-03
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS is the device name listed in this FDA 510(k) record. The listed applicant is J & B Assoc.. It received FDA 510(k) clearance on 1990-05-03 under 510(k) number K900520. 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 MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS?

MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS is a medical device that received FDA 510(k) clearance on 1990-05-03. The listed applicant is J & B Assoc.. The 510(k) number is K900520.

When did MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS receive FDA 510(k) clearance?

MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS received FDA 510(k) clearance on 1990-05-03, under 510(k) number K900520.

Who is the listed applicant for MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS?

The FDA 510(k) record lists J & B Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS?

The FDA product code for MODEL N742 SUNGLASSES W/ACRYLIC NIGHT DRIVER LENS is HQY.

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Other records listing J & B Assoc. 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.

K900524MODEL F3 FLIP UP SUNGLASSES W/POLORIZED COMPUTERK900527MODEL S139029 SUNGLASSES W/MIRROR ACRYLIC LENSESK900528MODEL 8806 SD SUNGLASSES W/ACRYLIC LENSESK900529MODEL 9018 PC SUNGLASSES W/POLYCARBONATE LENSESK900526MODEL F 1 FLIP-UP SUNGLASSES W/POLORIZED LENSK900521MODEL N742 SUNGLASSES W/POLYCARBONATE BLUE BLOCKER

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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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