K220891
- 510(k) number
- K220891
- Device name
- Kahook Dual Blade Glide (KDB Glide)
- Applicant
- New World Medical, Inc. CA · US
- Product code
- QUQ — Knife, Intraocular Pressure Lowering
- Decision date
- 2024-05-17
- Date received
- 2022-03-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K220891.pdf
Official FDA record: K220891
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.