SterilContainer with PrimeLine Pro Lid— 510(k) K172850

Name: FDA 510(k) clearance K172850
Creator: U.S. Food and Drug Administration
Published: 2017-11-17

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K172850 for SterilContainer with PrimeLine Pro Lid, Substantially Equivalent on 2017-11-17. Applicant: Aesculap, Inc.. Device class: 2.

Clearance details

Applicant: Aesculap, Inc.
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 2017-09-20
Decision date: 2017-11-17
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.