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FDA 510(k)

NU-VISION DISP. OPHTHALMIC DRESSING TRAY

K-Number: K801822 · 1980-09-30

ApplicantSummit Optics, Inc.
Decision Date1980-09-30
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NU-VISION DISP. OPHTHALMIC DRESSING TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Summit Optics, Inc.. It received FDA 510(k) clearance on 1980-09-30 under 510(k) number K801822. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NU-VISION DISP. OPHTHALMIC DRESSING TRAY?

NU-VISION DISP. OPHTHALMIC DRESSING TRAY is a medical device that received FDA 510(k) clearance on 1980-09-30. The listed applicant is Summit Optics, Inc.. The 510(k) number is K801822.

When did NU-VISION DISP. OPHTHALMIC DRESSING TRAY receive FDA 510(k) clearance?

NU-VISION DISP. OPHTHALMIC DRESSING TRAY received FDA 510(k) clearance on 1980-09-30, under 510(k) number K801822.

Who is the listed applicant for NU-VISION DISP. OPHTHALMIC DRESSING TRAY?

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

What is the FDA product code for NU-VISION DISP. OPHTHALMIC DRESSING TRAY?

The FDA product code for NU-VISION DISP. OPHTHALMIC DRESSING TRAY is KYG.

Related Clinical Trials

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Other records listing Summit Optics, 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.

K871800SUMMIT OPTICS POST-MYDRIATIC SPECTACLES

Related Devices (Code: KYG)

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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K974561MOISTAIR FLUID AIR TUBING SETAmerican Medical Devices, 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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