K230239
- 510(k) number
- K230239
- Device name
- AirSeal iFS System; AirSeal dV Solution
- Applicant
- Conmed Corporation NY · US
- Product code
- HIF — Insufflator, Laparoscopic
- Decision date
- 2023-09-20
- Date received
- 2023-01-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Obstetrics/Gynecology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K230239.pdf
Official FDA record: K230239
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.