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FDA 510(k)

VISITEC CANALICULAR STENT

K-Number: K915809 · 1992-02-24

ApplicantVisitec Co.
Decision Date1992-02-24
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

VISITEC CANALICULAR STENT is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1992-02-24 under 510(k) number K915809. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISITEC CANALICULAR STENT?

VISITEC CANALICULAR STENT is a medical device that received FDA 510(k) clearance on 1992-02-24. The listed applicant is Visitec Co.. The 510(k) number is K915809.

When did VISITEC CANALICULAR STENT receive FDA 510(k) clearance?

VISITEC CANALICULAR STENT received FDA 510(k) clearance on 1992-02-24, under 510(k) number K915809.

Who is the listed applicant for VISITEC CANALICULAR STENT?

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

What is the FDA product code for VISITEC CANALICULAR STENT?

The FDA product code for VISITEC CANALICULAR STENT is LZU.

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Other records listing Visitec Co. 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.

K953394VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}K945114VISITEC SCLERAL PLUGK945738VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPEK945172VISITEC SILICONE RETINAL IMPLANTS/EXPLANTSK942234VISITEC PRECISE-POINTK934269FIBEROPTIC ILLUMINATED INSTRUMENTS

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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

View on FDA Database →

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

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