MICRORUPTER V— 510(k) K023045

Substantially Equivalent

Meridian AG

FDA 510(k) clearance K023045 for MICRORUPTER V, Substantially Equivalent on 2002-09-26. Applicant: Meridian AG. Device class: 2.

Clearance details

Applicant: Meridian AG
Product code: Code LXS
Device class: Class 2
Regulation: 21 CFR 886.4392
Advisory panel: Ophthalmic
Date received: 2002-09-12
Decision date: 2002-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Thun, Bern, CH

Download summary PDF View on FDA.gov ↗

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