K231107
- 510(k) number
- K231107
- Device name
- Bronchoscope System
- Applicant
- Hunan Endoso Life Technology Co., Ltd. CN
- Product code
- EOQ — Bronchoscope (Flexible Or Rigid)
- Decision date
- 2024-02-15
- Date received
- 2023-04-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K231107.pdf
Official FDA record: K231107
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.