Ksea Scb-Rui Sco
FDA 510(k) K003113 · KARL STORZ Endoscopy-America, Inc.
510(k) numberK003113
Submission
- Device name
- Ksea Scb-Rui Sco
- Applicant
- KARL STORZ Endoscopy-America, Inc.
Culver City, CA, US - Received
- October 4, 2000
- Decision date
- March 27, 2001
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FET – Endoscopic Video Imaging System/Component, Gastroenterology-Urology
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1500
- Specialty
- Gastroenterology, Urology
To allow for visualization of body cavities through an endoscope by projecting images to a monitor.
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| K242067 | Visera Elite III Video System Center Olympus OTV-S700; Visera Elite III LED Light Source…FET · Traditional | Olympus Corporations of the Americas | 04/02/2025SE |
| K243321 | Endoscopic Video Image Processor (RP-IPD-V1000F)FET · Traditional | Guangzhou Red Pine Medical Instrument Co., Ltd. | 02/07/2025SE |
| K241532 | Flexible Video-Choledo-Cysto-Ureteroscope System (PL-2100)FET · Traditional | Shanghai SeeGen Photoelectric Technology Co., Ltd. | 10/22/2024SE |
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Questions and answers
When was Ksea Scb-Rui Sco cleared by the FDA?
Ksea Scb-Rui Sco (K003113) received a 510(k) decision of Substantially Equivalent on March 27, 2001, 174 days after the submission was received.
What is the product code of K003113?
The FDA product code is FET – Endoscopic Video Imaging System/Component, Gastroenterology-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.1500.