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FDA 510(k)

M.P.I. LENS GLIDE

K-Number: K792066 · 1980-01-29

ApplicantJ. Leon Bilby
Decision Date1980-01-29
Product CodeKYB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

M.P.I. LENS GLIDE is the device name listed in this FDA 510(k) record. The listed applicant is J. Leon Bilby. It received FDA 510(k) clearance on 1980-01-29 under 510(k) number K792066. The device is classified under product code KYB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M.P.I. LENS GLIDE?

M.P.I. LENS GLIDE is a medical device that received FDA 510(k) clearance on 1980-01-29. The listed applicant is J. Leon Bilby. The 510(k) number is K792066.

When did M.P.I. LENS GLIDE receive FDA 510(k) clearance?

M.P.I. LENS GLIDE received FDA 510(k) clearance on 1980-01-29, under 510(k) number K792066.

Who is the listed applicant for M.P.I. LENS GLIDE?

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

What is the FDA product code for M.P.I. LENS GLIDE?

The FDA product code for M.P.I. LENS GLIDE is KYB.

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Related Devices (Code: KYB)

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.

K081382DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786Duckworth & Kent, Ltd.K072985DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2Duckworth & Kent, Ltd.K070669IOL INJECTOR SETMedicel AGK063155MONARCH III IOL DELIVERY SYSTEMAlcon Manufacturing, Ltd.K063694AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28Bausch & Lomb, Inc.K032412RE-USEABLE MICROSTAAR INJECTOR, MSI-SStaar Surgical Co.

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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