Disposable guides KDNG00
FDA 510(k) K180970 · Koelis
510(k) numberK180970
Submission
- Device name
- Disposable guides KDNG00
- Applicant
- Koelis
Meylan, FR - Received
- April 13, 2018
- Decision date
- July 10, 2018
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code ITX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261170 | BA-004CCITX · Traditional | Fujifilm Corporation | 08/12/2026SE |
| K254143 | EM-TECH Passive Ultrasound Probe StrapITX · Traditional | EM-TECH Solutions, Inc. | 08/10/2026SE |
| K260161 | SmartGuide Disposable Guides and GridsITX · Traditional | UC-CARE , Ltd. | 07/30/2026SE |
| K262474 | ND Needle Guidance SystemITX · Traditional | Accurate Access, LLC | 07/27/2026SE |
| K261014 | Accuro® 3S Needle Guide KitITX · Traditional | Rivanna Medical, Inc. | 07/24/2026SE |
| K250883 | Ultrasonic Probe UM-3R (UM-3R); Ultrasonic Probe UM-G20-29R (UM-G20-29R)ITX · Traditional | Olympus Medical Systems Corporation | 09/18/2025SE |
| K250762 | Ultrasonic Probe UM-S20-17S (UM-S20-17S); Ultrasonic Probe UM-S20-20R (UM-S20-20R)ITX · Traditional | Olympus Medical Systems Corporation | 07/11/2025SE |
| K250524 | Mendaera Guidance SystemITX · Traditional | Mendaera, Inc. | 07/02/2025SE |
| K250469 | Accuro® 3S Needle Guide KitITX · Traditional | Rivanna Medical, Inc. | 06/13/2025SE |
| K241662 | Ultrasound Transducer CoverITX · Traditional | Vitrolife Sweden AB | 08/30/2024SE |
More from Vitrolife Sweden AB
| 510(k) | Device | Decision |
|---|---|---|
| K171040 | Reusable guides ranges (PERINE range, NAIL range, CON-LEAD range and LIN-LEAD range) and…ITX · Traditional | 07/31/2017SE |
| K170521 | TRINITY/3D Prostate SuiteIYN · Traditional | 05/30/2017SE |
| K160357 | TrinityIYN · Traditional | 05/02/2016SE |
| K141334 | Reusable GuideITX · Traditional | 07/11/2014SE |
| K131448 | 3D Prostate Suite 3DTRUS Prostate Mapping, MRI/3DTRUS Fusion Option, Second Look 3DTRUS…LLZ · Traditional | 07/26/2013SE |
| K100793 | Urostation 3D Prostate SuiteLLZ · Traditional | 09/22/2010SE |
Questions and answers
When was Disposable guides KDNG00 cleared by the FDA?
Disposable guides KDNG00 (K180970) received a 510(k) decision of Substantially Equivalent on July 10, 2018, 88 days after the submission was received.
What is the product code of K180970?
The FDA product code is ITX – Transducer, Ultrasonic, Diagnostic, a Class II (moderate risk) device regulated under 21 CFR 892.1570.