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FDA 510(k)

FRAME SPECTACLE

K-Number: K934858 · 1993-12-08

ApplicantArno Intl., Inc.
Decision Date1993-12-08
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FRAME SPECTACLE is the device name listed in this FDA 510(k) record. The listed applicant is Arno Intl., Inc.. It received FDA 510(k) clearance on 1993-12-08 under 510(k) number K934858. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRAME SPECTACLE?

FRAME SPECTACLE is a medical device that received FDA 510(k) clearance on 1993-12-08. The listed applicant is Arno Intl., Inc.. The 510(k) number is K934858.

When did FRAME SPECTACLE receive FDA 510(k) clearance?

FRAME SPECTACLE received FDA 510(k) clearance on 1993-12-08, under 510(k) number K934858.

Who is the listed applicant for FRAME SPECTACLE?

The FDA 510(k) record lists Arno Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FRAME SPECTACLE?

The FDA product code for FRAME SPECTACLE is HQZ.

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 Arno Intl., Inc. 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.

K934859CONTACT LENSES

Related Devices (Code: HQZ)

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.

K952597VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEWPoint of View Optical Outlet, Inc.K944313SPECTACLE FRAMESun Hing Optical Manufactory , Ltd.K945392SPECTACLE FRAMESeo Han Corp., Ltd.K945770OPTICAL FRAMESRamada Optics, Inc.K945176SPECTACLE FRAME OR EYEGLASS FRAMESOptipia Trading Co.K945350FRAME, SPECTACLESTaiwan Eva Industrial Co., Inc.

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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