MARTIN-HENSLEY SEGMENT LENS— 510(k) K897021

Name: FDA 510(k) clearance K897021
Creator: U.S. Food and Drug Administration
Published: 1990-06-22

Substantially Equivalent

Bruce W. Martin O.D. and Edward Hensley

FDA 510(k) clearance K897021 for MARTIN-HENSLEY SEGMENT LENS, Substantially Equivalent on 1990-06-22. Applicant: Bruce W. Martin O.D. and Edward Hensley. Device class: Unclassified.

Clearance details

Applicant: Bruce W. Martin O.D. and Edward Hensley
Product code: Code HPX
Device class: Unclassified
Advisory panel: Unknown
Date received: 1989-12-19
Decision date: 1990-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gladwin, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HPX

view all

K955777 — PMMA CLASIC1996-05-16
K940106 — KERATOPLASTY SUTURING LENS1994-05-25
K913081 — MULTI-VIEW BIFOCALS1991-10-23
K895411 — OPTIKEM PMMA CONTACT LENS1990-02-27
K874591 — ILLUMINATING INFUSION CONTACT LENS FOR EYE SURGERY1988-05-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.