SterilContainer S System
K-Number: K182032 · 2018-12-21
ApplicantAesculap, Inc.
Decision Date2018-12-21
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
SterilContainer S System is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2018-12-21 under approval number K182032. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SterilContainer S System?
SterilContainer S System is a medical device that received FDA 510(k) clearance on 2018-12-21. It is manufactured by Aesculap, Inc.. The 510(k) number is K182032.
When was SterilContainer S System approved by the FDA?
SterilContainer S System received FDA 510(k) clearance on 2018-12-21, under approval number K182032.
What company makes SterilContainer S System?
SterilContainer S System is manufactured by Aesculap, Inc..
What is the FDA product code for SterilContainer S System?
The FDA product code for SterilContainer S System is KCT.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.