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FDA 510(k)

EV MONOCANALICULAR STENT (TM)

K-Number: K883233 · 1988-08-22

ApplicantEagle Vision, Inc.
Decision Date1988-08-22
Product CodeOKS
DecisionSubstantially Equivalent

Device Summary

EV MONOCANALICULAR STENT (TM) 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 1988-08-22 under 510(k) number K883233. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EV MONOCANALICULAR STENT (TM)?

EV MONOCANALICULAR STENT (TM) is a medical device that received FDA 510(k) clearance on 1988-08-22. The listed applicant is Eagle Vision, Inc.. The 510(k) number is K883233.

When did EV MONOCANALICULAR STENT (TM) receive FDA 510(k) clearance?

EV MONOCANALICULAR STENT (TM) received FDA 510(k) clearance on 1988-08-22, under 510(k) number K883233.

Who is the listed applicant for EV MONOCANALICULAR STENT (TM)?

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 EV MONOCANALICULAR STENT (TM)?

The FDA product code for EV MONOCANALICULAR STENT (TM) is OKS.

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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 PLUGK890919TEMPORARY INTRACANALICULAR COLLAGEN IMPLANTK890920EAGLE VISION-FREEMAN(TM) PUNCTAL VALVE

View all 7 devices →

Related Devices (Code: OKS)

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.

K201892Ritleng®+ and Ritleng®+ PVPFci (France Chirurgie Instrumentation) SasK201606LacriJet®Fci (France Chirurgie Instrumentation) SasK170247Lacriflow CLKaneka Pharma America, LLCK161373NunchakuFci (France Chirurgie Instrumentation)K160710Oasis Lacrimal Intubation SetAnodyneK130375SELF-RETAINING BICANALICULUS INTUBATON SET IIFci Sas (France Chirurgie Instrumentation)

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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