REMOVER, SOFT-SERT CONTACT LENS— 510(k) K782140

Name: FDA 510(k) clearance K782140
Creator: U.S. Food and Drug Administration
Published: 1979-02-12

Substantially Equivalent

Mcmurray and Pendergost

FDA 510(k) clearance K782140 for REMOVER, SOFT-SERT CONTACT LENS, Substantially Equivalent on 1979-02-12. Applicant: Mcmurray and Pendergost. Device class: 1.

Clearance details

Applicant: Mcmurray and Pendergost
Product code: Code KYE
Device class: Class 1
Regulation: 21 CFR 886.5420
Advisory panel: Ophthalmic
Date received: 1978-12-27
Decision date: 1979-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KYE

view all

K872567 — SOFT CONTACT LENS REMOVER1987-08-10
K872591 — HARD CONTACT LENS REMOVER. ITEM #2891987-08-04
K871130 — CONTACT LENS TWEEZERS1987-05-12
K870072 — SUMMIT OPTICS CONTACT LENS REMOVER1987-02-12
K850983 — MARLIN SOFT LENS TWEEZER1985-09-10

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