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FDA 510(k)

SterilContainer with PrimeLine Pro Lid

K-Number: K172850 · 2017-11-17

ApplicantAesculap, Inc.
Decision Date2017-11-17
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SterilContainer with PrimeLine Pro Lid is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2017-11-17 under approval number K172850. 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 with PrimeLine Pro Lid?

SterilContainer with PrimeLine Pro Lid is a medical device that received FDA 510(k) clearance on 2017-11-17. It is manufactured by Aesculap, Inc.. The 510(k) number is K172850.

When was SterilContainer with PrimeLine Pro Lid approved by the FDA?

SterilContainer with PrimeLine Pro Lid received FDA 510(k) clearance on 2017-11-17, under approval number K172850.

What company makes SterilContainer with PrimeLine Pro Lid?

SterilContainer with PrimeLine Pro Lid is manufactured by Aesculap, Inc..

What is the FDA product code for SterilContainer with PrimeLine Pro Lid?

The FDA product code for SterilContainer with PrimeLine Pro Lid is KCT.

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Related Devices (Code: 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.

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