K242762
- 510(k) number
- K242762
- Device name
- Aesculap Aicon® Series Container System
- Applicant
- Aesculap, Inc. PA · US
- Product code
- KCT — Sterilization Wrap Containers, Trays, Cassettes & Ot
- Decision date
- 2025-05-13
- Date received
- 2024-09-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K242762.pdf
Official FDA record: K242762
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.