LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02)— 510(k) K221385
Substantially EquivalentOvesco Endoscopy AG
FDA 510(k) clearance K221385 for LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02), Substantially Equivalent on 2022-08-11. Applicant: Ovesco Endoscopy AG. Device class: 2.
Clearance details
- Applicant
- Ovesco Endoscopy AG
- Product code
- Code PLL
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tuebingen, DE
Recent devices under product code PLL
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