510(k) K214041

Device
Aesculap AICON Container
Applicant
Aesculap, Inc.
510(k) number
K214041
Product code
KCT
Decision
Substantially Equivalent (SESE)
Decision date
2022-12-30
Date received
2021-12-23
Regulation
880.6850
Classification name
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Omunique (Nikki) Luke
Address
3773 Corporate Pkwy. Center Valley PA US 18034 18034

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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