K232401
- 510(k) number
- K232401
- Device name
- Disposable Veress Needles
- Applicant
- Hangzhou Kangji Medical Instrument Co., Ltd. CN
- Product code
- HIF — Insufflator, Laparoscopic
- Decision date
- 2023-12-14
- Date received
- 2023-08-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232401.pdf
Official FDA record: K232401
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.