ERMIS STERILIZATION CONTAINER SYSTEM— 510(k) K123234

Name: FDA 510(k) clearance K123234
Creator: U.S. Food and Drug Administration
Published: 2013-07-05

Substantially Equivalent

Ermis Medizintechnik

FDA 510(k) clearance K123234 for ERMIS STERILIZATION CONTAINER SYSTEM, Substantially Equivalent on 2013-07-05. Applicant: Ermis Medizintechnik. Device class: 2.

Clearance details

Applicant: Ermis Medizintechnik
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 2012-10-15
Decision date: 2013-07-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mühlheim An Der Donau, DE

Download summary PDF View on FDA.gov ↗

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