AIMAGO EASYLDI MICROCIRCULATION CAMERA— 510(k) K121429

Name: FDA 510(k) clearance K121429
Creator: U.S. Food and Drug Administration
Published: 2012-08-10

Substantially Equivalent

Aimago SA

FDA 510(k) clearance K121429 for AIMAGO EASYLDI MICROCIRCULATION CAMERA, Substantially Equivalent on 2012-08-10. Applicant: Aimago SA. Device class: 2.

Clearance details

Applicant: Aimago SA
Product code: Code DPT
Device class: Class 2
Regulation: 21 CFR 870.2120
Advisory panel: Cardiovascular
Date received: 2012-05-14
Decision date: 2012-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lausanne, CH

Download summary PDF View on FDA.gov ↗

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