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FDA 510(k)

YON'S JAY ENTERPRISE CO

K-Number: K940730 · 1994-04-12

ApplicantYon'S Jay Enterprise Co.
Decision Date1994-04-12
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

YON'S JAY ENTERPRISE CO is the device name listed in this FDA 510(k) record. The listed applicant is Yon'S Jay Enterprise Co.. It received FDA 510(k) clearance on 1994-04-12 under 510(k) number K940730. 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 YON'S JAY ENTERPRISE CO?

YON'S JAY ENTERPRISE CO is a medical device that received FDA 510(k) clearance on 1994-04-12. The listed applicant is Yon'S Jay Enterprise Co.. The 510(k) number is K940730.

When did YON'S JAY ENTERPRISE CO receive FDA 510(k) clearance?

YON'S JAY ENTERPRISE CO received FDA 510(k) clearance on 1994-04-12, under 510(k) number K940730.

Who is the listed applicant for YON'S JAY ENTERPRISE CO?

The FDA 510(k) record lists Yon'S Jay Enterprise Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YON'S JAY ENTERPRISE CO?

The FDA product code for YON'S JAY ENTERPRISE CO is HQY.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Yon'S Jay Enterprise Co. 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.

K940725NONE-GENERIC

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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