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FDA 510(k)

ARNET OR ARNETTE

K-Number: K960530 · 1996-03-04

ApplicantArnet Optic Illusions
Decision Date1996-03-04
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ARNET OR ARNETTE is the device name listed in this FDA 510(k) record. The listed applicant is Arnet Optic Illusions. It received FDA 510(k) clearance on 1996-03-04 under 510(k) number K960530. 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 ARNET OR ARNETTE?

ARNET OR ARNETTE is a medical device that received FDA 510(k) clearance on 1996-03-04. The listed applicant is Arnet Optic Illusions. The 510(k) number is K960530.

When did ARNET OR ARNETTE receive FDA 510(k) clearance?

ARNET OR ARNETTE received FDA 510(k) clearance on 1996-03-04, under 510(k) number K960530.

Who is the listed applicant for ARNET OR ARNETTE?

The FDA 510(k) record lists Arnet Optic Illusions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARNET OR ARNETTE?

The FDA product code for ARNET OR ARNETTE 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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