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FDA 510(k)

TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT

K-Number: K890919 · 1989-05-16

ApplicantEagle Vision, Inc.
Decision Date1989-05-16
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Eagle Vision, Inc.. It received FDA 510(k) clearance on 1989-05-16 under 510(k) number K890919. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT?

TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT is a medical device that received FDA 510(k) clearance on 1989-05-16. The listed applicant is Eagle Vision, Inc.. The 510(k) number is K890919.

When did TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT receive FDA 510(k) clearance?

TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT received FDA 510(k) clearance on 1989-05-16, under 510(k) number K890919.

Who is the listed applicant for TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT?

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

What is the FDA product code for TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT?

The FDA product code for TEMPORARY INTRACANALICULAR COLLAGEN IMPLANT is LZU.

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Other records listing Eagle Vision, 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.

K053333EAGLEVISION GELLANSERTS, MODEL REF 0040K030353MONOCANALICULAR STENTS, LACRIMAL INTUBATION SETSK991130FLEXPLUGK905427EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUGK890920EAGLE VISION-FREEMAN(TM) PUNCTAL VALVEK883233EV MONOCANALICULAR STENT (TM)

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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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