Cleared Traditional

SIASCOPE V

K062736 · Astron Clinica Limited · General & Plastic Surgery
Sep 2007
Decision
366d
Days
Class 2
Risk

About This 510(k) Submission

K062736 is an FDA 510(k) clearance for the SIASCOPE V, a Light Based Imaging (Class II — Special Controls, product code PSN), submitted by Astron Clinica Limited (Crofton, US). The FDA issued a Cleared decision on September 14, 2007, 366 days after receiving the submission on September 13, 2006. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4580.

Submission Details

510(k) Number K062736 FDA.gov
FDA Decision Cleared SESE
Date Received September 13, 2006
Decision Date September 14, 2007
Days to Decision 366 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code PSN — Light Based Imaging
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4580
Definition Emission And Collection Of Light To Create An Image For Medical Purposes