GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING— 510(k) K001125

Name: FDA 510(k) clearance K001125
Creator: U.S. Food and Drug Administration
Published: 2000-10-04

Substantially Equivalent

Geuder GmbH

FDA 510(k) clearance K001125 for GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING, Substantially Equivalent on 2000-10-04. Applicant: Geuder GmbH. Device class: 1.

Clearance details

Applicant: Geuder GmbH
Product code: Code NCE
Device class: Class 1
Regulation: 21 CFR 886.4300
Advisory panel: Ophthalmic
Date received: 2000-04-07
Decision date: 2000-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Centercille, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NCE

view all

K042478 — CAPSULE TENSION RING INSERTER, MODEL 7-8102004-12-28
K011498 — EASY CONTROL MICRO INSERTER, MODEL ON3852001-07-09

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