K222783
- 510(k) number
- K222783
- Device name
- MD Mattress Suture Placement Device
- Applicant
- Lsi Solutions, Inc. NY · US
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2024-01-12
- Date received
- 2022-09-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K222783.pdf
Official FDA record: K222783
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.