HARD CONTACT LENS REMOVER. ITEM #289— 510(k) K872591

Name: FDA 510(k) clearance K872591
Creator: U.S. Food and Drug Administration
Published: 1987-08-04

Substantially Equivalent

Magnivision, Inc.

FDA 510(k) clearance K872591 for HARD CONTACT LENS REMOVER. ITEM #289, Substantially Equivalent on 1987-08-04. Applicant: Magnivision, Inc.. Device class: 1.

Clearance details

Applicant: Magnivision, Inc.
Product code: Code KYE
Device class: Class 1
Regulation: 21 CFR 886.5420
Advisory panel: Ophthalmic
Date received: 1987-07-01
Decision date: 1987-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KYE

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K872567 — SOFT CONTACT LENS REMOVER1987-08-10
K871130 — CONTACT LENS TWEEZERS1987-05-12
K870072 — SUMMIT OPTICS CONTACT LENS REMOVER1987-02-12
K850983 — MARLIN SOFT LENS TWEEZER1985-09-10
K850984 — MARLIN SOFT LENS HANDLER1985-09-10

More clearances from Magnivision, Inc.

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K900777 — ITEM #273 CONTACT LENS CASES1990-03-30
K900778 — ITEM #272 MAGNIF-EYES CONTACT LENS CASE1990-03-30
K897084 — CONFEES(R)+ CONTACT LENS HOLDER1990-02-28
K897085 — COMFEES(R) + CON-PAK(TM) LENS CASE1990-02-28
K882384 — DELUXE CONTACT LENS HOLDER (HARD & SOFT) #2831989-06-23

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