EUROMI EVA SP6— 510(k) K101413

Substantially Equivalent

Euromi S.A

FDA 510(k) clearance K101413 for EUROMI EVA SP6, Substantially Equivalent on 2010-12-16. Applicant: Euromi S.A. Device class: 2.

Clearance details

Applicant
Euromi S.A
Product code
Code QPB
Device class
Class 2
Regulation
21 CFR 878.5040
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Shelton, CT, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.