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)

EYECOTECH CORP

K-Number: K941414 · 1994-07-12

ApplicantEyecotech Corp.
Decision Date1994-07-12
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EYECOTECH CORP is the device name listed in this FDA 510(k) record. The listed applicant is Eyecotech Corp.. It received FDA 510(k) clearance on 1994-07-12 under 510(k) number K941414. 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 EYECOTECH CORP?

EYECOTECH CORP is a medical device that received FDA 510(k) clearance on 1994-07-12. The listed applicant is Eyecotech Corp.. The 510(k) number is K941414.

When did EYECOTECH CORP receive FDA 510(k) clearance?

EYECOTECH CORP received FDA 510(k) clearance on 1994-07-12, under 510(k) number K941414.

Who is the listed applicant for EYECOTECH CORP?

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

What is the FDA product code for EYECOTECH CORP?

The FDA product code for EYECOTECH CORP 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

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.K945176SPECTACLE FRAME OR EYEGLASS FRAMESOptipia Trading Co.K945770OPTICAL FRAMESRamada Optics, Inc.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.

↑