Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter)— 510(k) K151474
Substantially EquivalentFujifilm Medical System U.S.A., Inc.
FDA 510(k) clearance K151474 for Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter), Substantially Equivalent on 2016-02-18. Applicant: Fujifilm Medical System U.S.A., Inc..
Clearance details
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Product code
- Code KGE
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wayne, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.