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)

SPLASHMASTER PRESCRIPTION EYEWEAR

K-Number: K935903 · 1994-02-22

ApplicantCabot Safety Corp.
Decision Date1994-02-22
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPLASHMASTER PRESCRIPTION EYEWEAR is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Safety Corp.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K935903. 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 SPLASHMASTER PRESCRIPTION EYEWEAR?

SPLASHMASTER PRESCRIPTION EYEWEAR is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Cabot Safety Corp.. The 510(k) number is K935903.

When did SPLASHMASTER PRESCRIPTION EYEWEAR receive FDA 510(k) clearance?

SPLASHMASTER PRESCRIPTION EYEWEAR received FDA 510(k) clearance on 1994-02-22, under 510(k) number K935903.

Who is the listed applicant for SPLASHMASTER PRESCRIPTION EYEWEAR?

The FDA 510(k) record lists Cabot Safety Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPLASHMASTER PRESCRIPTION EYEWEAR?

The FDA product code for SPLASHMASTER PRESCRIPTION EYEWEAR 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 Cabot Safety Corp. 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.

K941147SPLASHMASTER OC EYE AND FACE PROTECTIVE PRODUCTSK935723SPLASHMASTER FACE PROTECTIVE PRODUCTS (TUFFSHIELD FACESHIELD, VISTACLEAR FACESHIELD)

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.

↑