K240994
- 510(k) number
- K240994
- Device name
- Nexpowder
- Applicant
- Nextbiomedical Co., Ltd. KR
- Product code
- QAU — Hemostatic Device For Endoscopic Gastrointestinal Us
- Decision date
- 2024-11-27
- Date received
- 2024-04-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K240994.pdf
Official FDA record: K240994
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.