K232072
- 510(k) number
- K232072
- Device name
- AMICA-GEN AGN-H-1.3, AMICA-GEN AGN 3.3, AMICA-PROBE 17G & 18G
- Applicant
- H.S Hospital Service S.P.A IT
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-02-09
- Date received
- 2023-07-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K232072.pdf
Official FDA record: K232072
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.