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.. Device class: 2.
Clearance details
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Product code
- Code KGE
- Device class
- Class 2
- Regulation
- 21 CFR 876.4300
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wayne, NJ, US
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More clearances from Fujifilm Medical System U.S.A., Inc.
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