STERILCONTAINER SYSTEM— 510(k) K112671

Substantially Equivalent

Aesculap, Ltd.

FDA 510(k) clearance K112671 for STERILCONTAINER SYSTEM, Substantially Equivalent on 2012-05-04. Applicant: Aesculap, Ltd.. Device class: 2.

Clearance details

Applicant: Aesculap, Ltd.
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 2011-09-14
Decision date: 2012-05-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Center Valley, PA, US

Download summary PDF View on FDA.gov ↗

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