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FDA 510(k)

INTELIPORT OCCLUDING DEVICE

K-Number: K040231 · 2004-07-13

ApplicantAlcon, Inc.
Decision Date2004-07-13
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

INTELIPORT OCCLUDING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Alcon, Inc.. It received FDA 510(k) clearance on 2004-07-13 under 510(k) number K040231. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTELIPORT OCCLUDING DEVICE?

INTELIPORT OCCLUDING DEVICE is a medical device that received FDA 510(k) clearance on 2004-07-13. The listed applicant is Alcon, Inc.. The 510(k) number is K040231.

When did INTELIPORT OCCLUDING DEVICE receive FDA 510(k) clearance?

INTELIPORT OCCLUDING DEVICE received FDA 510(k) clearance on 2004-07-13, under 510(k) number K040231.

Who is the listed applicant for INTELIPORT OCCLUDING DEVICE?

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

What is the FDA product code for INTELIPORT OCCLUDING DEVICE?

The FDA product code for INTELIPORT OCCLUDING DEVICE is LZU.

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.

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Other records listing Alcon, Inc. as applicant

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.

K071236ALCON MULTI-PURPOSE SOLUTIONK031193SOFT (HYDROPHILIC) CONTACT LENS CARE SOLUTION

Related Devices (Code: LZU)

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.

K241229Hello,eyes® BIO PlugBio Optics Co., Ltd.K222164Visant Medical Canalicular PlugVisant Medical, Inc.K213988SOFT PLUG Extended Duration 180 Tapered Canalicular PlugOasis Medical, Inc.K190210Tear Pool Dissolvable Punctum PlugsAlphamed, Inc.K162361Soft Plug Extended Duration 180 Canalicular PlugOasis Medical, Inc.K161673LacriPro Punctum PlugLacrimedics, 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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