SUMMIT OPTICS CONTACT LENS REMOVER— 510(k) K870072

Name: FDA 510(k) clearance K870072
Creator: U.S. Food and Drug Administration
Published: 1987-02-12

Substantially Equivalent

Dayton Mfg. Co.

FDA 510(k) clearance K870072 for SUMMIT OPTICS CONTACT LENS REMOVER, Substantially Equivalent on 1987-02-12. Applicant: Dayton Mfg. Co.. Device class: 1.

Clearance details

Applicant: Dayton Mfg. Co.
Product code: Code KYE
Device class: Class 1
Regulation: 21 CFR 886.5420
Advisory panel: Ophthalmic
Date received: 1987-01-08
Decision date: 1987-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, 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
K850983 — MARLIN SOFT LENS TWEEZER1985-09-10
K850984 — MARLIN SOFT LENS HANDLER1985-09-10

More clearances from Dayton Mfg. Co.

view all

K870164 — SUMMIT OPTICS SOFT CONTACT LENS CASE1987-02-10

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