Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS

K-Number: K942951 · 1994-08-02

ApplicantThe Orvis Co., Inc.
Decision Date1994-08-02
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS is the device name listed in this FDA 510(k) record. The listed applicant is The Orvis Co., Inc.. It received FDA 510(k) clearance on 1994-08-02 under 510(k) number K942951. 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 ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS?

ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS is a medical device that received FDA 510(k) clearance on 1994-08-02. The listed applicant is The Orvis Co., Inc.. The 510(k) number is K942951.

When did ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS receive FDA 510(k) clearance?

ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS received FDA 510(k) clearance on 1994-08-02, under 510(k) number K942951.

Who is the listed applicant for ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS?

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

What is the FDA product code for ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS?

The FDA product code for ORVIS LIGHT WEIGHT POLARIZED CLIP-ONS 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 The Orvis Co., 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.

K950609ORVIS KEY WEST SUNGLASSESK943161ORVIS DRIVING GLASSESK943131ORVIS POLARIZED BI-FOCALSK942952ORVIS WORLD FINEST POLARIZED CLIP ONSK941910SUNGLASSESK941751SUNGLASSES

View all 9 devices →

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.

↑