M.P.I. LENS GLIDE— 510(k) K792066

Name: FDA 510(k) clearance K792066
Creator: U.S. Food and Drug Administration
Published: 1980-01-29

Substantially Equivalent

J. Leon Bilby

FDA 510(k) clearance K792066 for M.P.I. LENS GLIDE, Substantially Equivalent on 1980-01-29. Applicant: J. Leon Bilby. Device class: 1.

Clearance details

Applicant: J. Leon Bilby
Product code: Code KYB
Device class: Class 1
Regulation: 21 CFR 886.4300
Advisory panel: Ophthalmic
Date received: 1979-10-15
Decision date: 1980-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KYB

view all

K152357 — MicroSTAAR Injector System Cartridges2015-10-30
K081382 — DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK77862008-10-23
K072985 — DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-22008-06-20
K070669 — IOL INJECTOR SET2007-11-01
K063155 — MONARCH III IOL DELIVERY SYSTEM2007-03-27

Adverse events under product code KYB

product code KYB

Injury: 218
Malfunction: 1,989
Other: 1
Total: 2,208

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.