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FDA 510(k)

GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING

K-Number: K001125 · 2000-10-04

ApplicantGeuder GmbH
Decision Date2000-10-04
Product CodeNCE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING is the device name listed in this FDA 510(k) record. The listed applicant is Geuder GmbH. It received FDA 510(k) clearance on 2000-10-04 under 510(k) number K001125. The device is classified under product code NCE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING?

GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING is a medical device that received FDA 510(k) clearance on 2000-10-04. The listed applicant is Geuder GmbH. The 510(k) number is K001125.

When did GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING receive FDA 510(k) clearance?

GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING received FDA 510(k) clearance on 2000-10-04, under 510(k) number K001125.

Who is the listed applicant for GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING?

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

What is the FDA product code for GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING?

The FDA product code for GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING is NCE.

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Related Devices (Code: NCE)

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.

K042478CAPSULE TENSION RING INSERTER, MODEL 7-810Duckworth & Kent, Ltd.K011498EASY CONTROL MICRO INSERTER, MODEL ON385Ophtec USA, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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