K232519
- 510(k) number
- K232519
- Device name
- ENDOCOLLECT Specimen Retrieval Bag
- Applicant
- Ximedica RI · US
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2024-01-05
- Date received
- 2023-08-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232519.pdf
Official FDA record: K232519
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.