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FDA 510(k)

MARTIN-HENSLEY SEGMENT LENS

K-Number: K897021 · 1990-06-22

ApplicantBruce W. Martin O.D. and Edward Hensley
Decision Date1990-06-22
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

MARTIN-HENSLEY SEGMENT LENS is the device name listed in this FDA 510(k) record. The listed applicant is Bruce W. Martin O.D. and Edward Hensley. It received FDA 510(k) clearance on 1990-06-22 under 510(k) number K897021. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN-HENSLEY SEGMENT LENS?

MARTIN-HENSLEY SEGMENT LENS is a medical device that received FDA 510(k) clearance on 1990-06-22. The listed applicant is Bruce W. Martin O.D. and Edward Hensley. The 510(k) number is K897021.

When did MARTIN-HENSLEY SEGMENT LENS receive FDA 510(k) clearance?

MARTIN-HENSLEY SEGMENT LENS received FDA 510(k) clearance on 1990-06-22, under 510(k) number K897021.

Who is the listed applicant for MARTIN-HENSLEY SEGMENT LENS?

The FDA 510(k) record lists Bruce W. Martin O.D. and Edward Hensley as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARTIN-HENSLEY SEGMENT LENS?

The FDA product code for MARTIN-HENSLEY SEGMENT LENS is HPX.

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: HPX)

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.

K955777PMMA CLASICRand Scientific Corp.K940106KERATOPLASTY SUTURING LENSVisionary Technologies of Miami, Inc.K913081MULTI-VIEW BIFOCALSCamp Contact LensesK895411OPTIKEM PMMA CONTACT LENSOptikem Polymers, Inc.K874591ILLUMINATING INFUSION CONTACT LENS FOR EYE SURGERYVitreo Dynamics, Co.K865111CHARTER HARD CONTACT LENS CLEANING SOLUTIONPaco Pharmaceutical Services, 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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