RADSCAN EQUIPMENT SLICKER— 510(k) K101350

Name: FDA 510(k) clearance K101350
Creator: U.S. Food and Drug Administration
Published: 2011-01-04

Substantially Equivalent

Radscan Medical Equipment, Inc.

FDA 510(k) clearance K101350 for RADSCAN EQUIPMENT SLICKER, Substantially Equivalent on 2011-01-04. Applicant: Radscan Medical Equipment, Inc.. Device class: 2.

Clearance details

Applicant: Radscan Medical Equipment, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 2010-05-14
Decision date: 2011-01-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

Download summary PDF View on FDA.gov ↗

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