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FDA 510(k)

STERILCONTAINER SYSTEM

K-Number: K112671 · 2012-05-04

ApplicantAesculap, Ltd.
Decision Date2012-05-04
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILCONTAINER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Ltd.. It received FDA 510(k) clearance on 2012-05-04 under 510(k) number K112671. 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 SYSTEM?

STERILCONTAINER SYSTEM is a medical device that received FDA 510(k) clearance on 2012-05-04. The listed applicant is Aesculap, Ltd.. The 510(k) number is K112671.

When did STERILCONTAINER SYSTEM receive FDA 510(k) clearance?

STERILCONTAINER SYSTEM received FDA 510(k) clearance on 2012-05-04, under 510(k) number K112671.

Who is the listed applicant for STERILCONTAINER SYSTEM?

The FDA 510(k) record lists Aesculap, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILCONTAINER SYSTEM?

The FDA product code for STERILCONTAINER SYSTEM is KCT.

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Related Devices (Code: KCT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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