EchoTip Ultra® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes; EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes
FDA 510(k) K261274 · Cook Ireland, Ltd.
510(k) numberK261274
Submission
- Device name
- EchoTip Ultra® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes; EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes
- Applicant
- Cook Ireland, Ltd.
Limerick, IE - Received
- April 17, 2026
- Decision date
- July 24, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KTI – Bronchoscope Accessory
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 874.4680
- Specialty
- Ear, Nose, Throat
If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
Other 510(k)s with product code KTI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K251478 | ClearTip TBNA TypeKTI · Traditional | Finemedix Co., Ltd. | 04/16/2026SE |
| K254040 | LungFlow Basket CatheterKTI · Traditional | Free Flow Medical, Inc. | 03/12/2026SE |
| K251402 | LIA-1 Catheter (542-1)KTI · Traditional | Leadoptik, Inc. | 12/19/2025SE |
| K252874 | Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01KTI · Special | Serpex Medical, Inc. | 10/08/2025SE |
| K251664 | Single Use Aspiration Needle (NA-201SX-4021); Single Use Aspiration Needle (NA-201SX-4022)KTI · Traditional | Olympus Medical Systems Corporation | 07/29/2025SE |
| K250263 | Disposable Grasping Forceps FG-52D/FG-54DKTI · Traditional | Olympus Medical Systems Corp. | 03/31/2025SE |
| K241679 | Disposable Cytology Brush (AF series)KTI · Traditional | Alton (Shanghai) Medical Instruments Co., Ltd. | 03/04/2025SE |
| K231818 | METIC- Airway Balloon CatheterKTI · Traditional | M/S Meril Life Sciences Pvt. , Ltd. | 11/15/2023SE |
| K230778 | EndoCoreKTI · Traditional | Praxis Medical, LLC | 09/25/2023SE |
| K230280 | ANDORATE® Suction Valve and ANDORATE® Biopsy ValveKTI · Traditional | Ga Health Company Limited | 05/11/2023SE |
More from Ga Health Company Limited
| 510(k) | Device | Decision |
|---|---|---|
| K241209 | EchoTip AcuCore EUS Biopsy Needle (ECHO-BX-19)FCG · Traditional | 07/29/2024SE |
| K233079 | Zimmon® Pancreatic Stents/Stent sets (SPSOF, SPSOS, ZEPDF, ZEPDS, ZPSOF, ZPSOS); Geenen®…FGE · Traditional | 06/14/2024SE |
| K230909 | EchoTip® AcuCore Ultrasound Biopsy Needle (ECHO-BX-3-22)FCG · Traditional | 05/30/2023SE |
| K213946 | Compass BDS Biliary StentFGE · Traditional | 05/09/2022SE |
| K210476 | EchoTip Ultra Endoscopic Ultrasound Needle, EchoTip ProCore HD Ultrasound Biopsy Needle…FCG · Traditional | 05/20/2021SE |
| K182980 | Zilver 518 Biliary Stent, Zilver 635 Biliary StentFGE · Special | 11/16/2018SESU |
| K180868 | Nasal Biliary Drainage Set, Liguory Nasal Biliary Drainage Set, Nagaraja Nasal Biliary…FGE · Traditional | 07/06/2018SE |
| K172057 | Zimmon Pancreatic Stents/Stent sets, Geenen Pancreatic Stents/Stent Sets, Pushing…FGE · Traditional | 03/09/2018SE |
| K172044 | Cotton-Huibregtse Stent, Cotton-Leung Biliary Stent, Cotton-Leung Sof-Flex Biliary…FGE · Traditional | 02/27/2018SE |
| K171619 | 14Fr Colon Decompression Set, Macon Colon Decompression SetFEG · Traditional | 08/01/2017SE |
Questions and answers
When was EchoTip Ultra® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes; EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes cleared by the FDA?
EchoTip Ultra® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes; EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes (K261274) received a 510(k) decision of Substantially Equivalent on July 24, 2026, 98 days after the submission was received.
What is the product code of K261274?
The FDA product code is KTI – Bronchoscope Accessory, a Class II (moderate risk) device regulated under 21 CFR 874.4680.