K240754
- 510(k) number
- K240754
- Device name
- N2
- Applicant
- Megagen Implant Co., Ltd. KR
- Product code
- EIA — Unit, Operative Dental
- Decision date
- 2024-03-21
- Date received
- 2024-03-20
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Flag
- Third-party review
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K240754.pdf
Official FDA record: K240754
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.