KERATOPLASTY SUTURING LENS— 510(k) K802593

Name: FDA 510(k) clearance K802593
Creator: U.S. Food and Drug Administration
Published: 1980-12-22

Substantially Equivalent

Paris Contact Lens Laboratory

FDA 510(k) clearance K802593 for KERATOPLASTY SUTURING LENS, Substantially Equivalent on 1980-12-22. Applicant: Paris Contact Lens Laboratory. Device class: Unclassified.

Clearance details

Applicant: Paris Contact Lens Laboratory
Product code: Code HPX
Device class: Unclassified
Advisory panel: Unknown
Date received: 1980-10-21
Decision date: 1980-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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
K897021 — MARTIN-HENSLEY SEGMENT LENS1990-06-22
K895411 — OPTIKEM PMMA CONTACT LENS1990-02-27

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