BONASSE CONTACT LENS CASE— 510(k) K991206

Name: FDA 510(k) clearance K991206
Creator: U.S. Food and Drug Administration
Published: 2000-06-06

Substantially Equivalent

Bonasse Ent. Co., Ltd.

FDA 510(k) clearance K991206 for BONASSE CONTACT LENS CASE, Substantially Equivalent on 2000-06-06. Applicant: Bonasse Ent. Co., Ltd.. Device class: 2.

Clearance details

Applicant: Bonasse Ent. Co., Ltd.
Product code: Code LRX
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 1999-04-09
Decision date: 2000-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRX

view all

K252175 — LANDR Contact LENS Case2026-02-10
K250495 — MINI VP1 (PL67_F); MINI VP1 (PL61_F)2025-08-01
K240095 — CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)2024-10-09
K231123 — Phoenix Contact Lens Case - dome top flat pack (CL-01) +2 more2023-08-30
K173538 — Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODisc2017-12-04

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