DEFOGGING AND CLEANING SOLUTION- FLO-X— 510(k) K102452

Name: FDA 510(k) clearance K102452
Creator: U.S. Food and Drug Administration
Published: 2010-12-23

Substantially Equivalent

Minimally Invasive Devices, LLC

FDA 510(k) clearance K102452 for DEFOGGING AND CLEANING SOLUTION- FLO-X, Substantially Equivalent on 2010-12-23. Applicant: Minimally Invasive Devices, LLC. Device class: 2.

Clearance details

Applicant: Minimally Invasive Devices, LLC
Product code: Code OCT
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2010-08-27
Decision date: 2010-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Butler, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OCT

view all

K251068 — KnoxFog Anti-fogging Device2025-08-27
K231822 — GOLFF Sterile Anti-Fog Solution2024-02-26
K221293 — E-Brik Visualization Assistant2022-07-07
K190864 — Konix Anti-Fog Solution2020-08-27
K181887 — AMD Anti-Fog Solution2019-01-22

More clearances from Minimally Invasive Devices, LLC

view all

K080613 — CLEAR-VU SYSTEM, MODELS: CVL-01-1000, CVL-01-1030, CVL-01-10452008-11-06

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