CONTACT LENS REMOVER AND INSERTER— 510(k) K780663

Name: FDA 510(k) clearance K780663
Creator: U.S. Food and Drug Administration
Published: 1978-05-17

Substantially Equivalent

Dmv Contact Lens Co.

FDA 510(k) clearance K780663 for CONTACT LENS REMOVER AND INSERTER, Substantially Equivalent on 1978-05-17. Applicant: Dmv Contact Lens Co.. Device class: 1.

Clearance details

Applicant: Dmv Contact Lens Co.
Product code: Code KYE
Device class: Class 1
Regulation: 21 CFR 886.5420
Advisory panel: Ophthalmic
Date received: 1978-04-20
Decision date: 1978-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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
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

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K830496 — DMV ANGLER1983-03-09
K780664 — SOFT LENS REMOVER/INSERTER/MANIPULATOR1978-05-17

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