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FDA 510(k)

JJ Series Container System

K-Number: K192056 · 2020-03-27

ApplicantAesculap, Inc.
Decision Date2020-03-27
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JJ Series Container System is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2020-03-27 under approval number K192056. 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 JJ Series Container System?

JJ Series Container System is a medical device that received FDA 510(k) clearance on 2020-03-27. It is manufactured by Aesculap, Inc.. The 510(k) number is K192056.

When was JJ Series Container System approved by the FDA?

JJ Series Container System received FDA 510(k) clearance on 2020-03-27, under approval number K192056.

What company makes JJ Series Container System?

JJ Series Container System is manufactured by Aesculap, Inc..

What is the FDA product code for JJ Series Container System?

The FDA product code for JJ Series Container System is KCT.

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Related PubMed Literature

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Other Devices by Aesculap, Inc.

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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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