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FDA 510(k)

NONE-GENERIC

K-Number: K940726 · 1994-04-11

ApplicantJay-Y Enterprises Co., Inc.
Decision Date1994-04-11
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NONE-GENERIC is the device name listed in this FDA 510(k) record. The listed applicant is Jay-Y Enterprises Co., Inc.. It received FDA 510(k) clearance on 1994-04-11 under 510(k) number K940726. 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 NONE-GENERIC?

NONE-GENERIC is a medical device that received FDA 510(k) clearance on 1994-04-11. The listed applicant is Jay-Y Enterprises Co., Inc.. The 510(k) number is K940726.

When did NONE-GENERIC receive FDA 510(k) clearance?

NONE-GENERIC received FDA 510(k) clearance on 1994-04-11, under 510(k) number K940726.

Who is the listed applicant for NONE-GENERIC?

The FDA 510(k) record lists Jay-Y Enterprises Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NONE-GENERIC?

The FDA product code for NONE-GENERIC is HQY.

Related Clinical Trials

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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

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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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