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FDA 510(k)

Aesculap Aicon® Series Container System

K-Number: K242762 · 2025-05-13

ApplicantAesculap, Inc.
Decision Date2025-05-13
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Aesculap Aicon® Series Container System is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2025-05-13 under approval number K242762. 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 Aesculap Aicon® Series Container System?

Aesculap Aicon® Series Container System is a medical device that received FDA 510(k) clearance on 2025-05-13. It is manufactured by Aesculap, Inc.. The 510(k) number is K242762.

When was Aesculap Aicon® Series Container System approved by the FDA?

Aesculap Aicon® Series Container System received FDA 510(k) clearance on 2025-05-13, under approval number K242762.

What company makes Aesculap Aicon® Series Container System?

Aesculap Aicon® Series Container System is manufactured by Aesculap, Inc..

What is the FDA product code for Aesculap Aicon® Series Container System?

The FDA product code for Aesculap Aicon® Series Container System is KCT.

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Related PubMed Literature

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Other Devices by Aesculap, Inc.

K152960ELAN 4 Motor System K160393AdTec K151165Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture K172850SterilContainer with PrimeLine Pro Lid K173271Aesculap Slim Clip Applier Forceps K171001Monosyn Quick Synthetic Absorbable Surgical Suture

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Related Devices (Code: KCT)

K160574K3PRO SURGICAL TRAYArgon Med. Productions Vertriebs Gesellschaft Mbh CO KG K162600Jewel Precision Reusable Rigid Sterilization Container SystemJewel Precision Sheet Metal & Machine, Inc. K160912Sterilization TraySTERIS Corporation K161347Signia sterilization trayCovidien K152745ReNew Sterilization Trays(Catalog #3708 and #3709)Microline Surgical, Inc. K152111Symmetry Surgical Quad-Lock Container SystemSymmetry Surgical, Inc.

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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