K232880
- 510(k) number
- K232880
- Device name
- Inzii Ripstop Redeployable Retrieval System
- Applicant
- Applied Medical Resources Corporation CA · US
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2023-11-01
- Date received
- 2023-09-18
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232880.pdf
Official FDA record: K232880
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.