K242184
- 510(k) number
- K242184
- Device name
- Alcon 27GA Chandelier (8065000252); Alcon 27+ DS Wide Angle Endoilluminator (8065000253); Alcon 27+ DS Endoilluminator (8065000256);
- Applicant
- Alcon Laboratories, Inc. TX · US
- Product code
- MPA — Endoilluminator
- Decision date
- 2024-12-04
- Date received
- 2024-07-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242184.pdf
Official FDA record: K242184
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.