ZANZA-CLICK— 510(k) DEN130019

Unknown

Tecnimed S.R.L.

FDA 510(k) clearance DEN130019 for ZANZA-CLICK, Unknown on 2014-11-07. Applicant: Tecnimed S.R.L.. Device class: 2.

Clearance details

Applicant: Tecnimed S.R.L.
Product code: Code OSG
Device class: Class 2
Regulation: 21 CFR 882.5894
Advisory panel: Neurology
Date received: 2013-02-28
Decision date: 2014-11-07
Decision: Unknown
Clearance type: Direct
Location: Ormond Beach, FL, US

View on FDA.gov ↗

Recent devices under product code OSG

DEN100024 — ZAP-IT!2014-11-07

More clearances from Tecnimed S.R.L.

K160680 — VisioFocus Mini, VisioFocus Smart2017-04-19
K122412 — VISIOFOCUS2013-03-13
K072108 — MODIFICATION TO THERMOFOCUS 0800, 0900, 01500 AND 0700 SERIES2007-08-31
K033790 — THERMOFOCUS 0800, 0900, 01500 AND 0700 SERIES2004-06-03

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