The Biopsy Tool
FDA 510(k) K941563 · Citation Medical Corp.
510(k) numberK941563
Submission
- Device name
- The Biopsy Tool
- Applicant
- Citation Medical Corp.
Reno, NV, US - Received
- April 1, 1994
- Decision date
- September 26, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- FCG – Biopsy Needle
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1075
- Specialty
- Gastroenterology, Urology
Other 510(k)s with product code FCG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252646 | Single-Use Fine Needle Biopsy (FNB) device (NA-U210H)FCG · Traditional | Olympus Medical Systems Corp. | 10/24/2025SE |
| K250994 | ClearTip FNA and FNB TypesFCG · Traditional | Finemedix Co., Ltd. | 08/21/2025SE |
| K241209 | EchoTip AcuCore EUS Biopsy Needle (ECHO-BX-19)FCG · Traditional | Cook Ireland, Ltd. | 07/29/2024SE |
| K231422 | Precision GIFCG · Traditional | Limaca Medical, Ltd. | 08/28/2023SE |
| K231267 | ClearTipFCG · Traditional | Finemedix Co., Ltd. | 06/30/2023SE |
| K230909 | EchoTip® AcuCore Ultrasound Biopsy Needle (ECHO-BX-3-22)FCG · Traditional | Cook Ireland, Ltd. | 05/30/2023SE |
| K212423 | EndoDrill® Model XFCG · Traditional | Bibbinstruments AB | 03/29/2023SE |
| K212822 | Disposable Coaxial Biopsy NeedleFCG · Traditional | Suzhou Leapmed Healthcare Corporation | 07/06/2022SE |
| K212819 | Disposable Biopsy Refill NeedleFCG · Traditional | Suzhou Leapmed Healthcare Corporation | 07/06/2022SE |
| K210476 | EchoTip Ultra Endoscopic Ultrasound Needle, EchoTip ProCore HD Ultrasound Biopsy Needle…FCG · Traditional | Cook Ireland, Ltd. | 05/20/2021SE |
More from Cook Ireland, Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K951941 | Citation Multiple Use Delta ScopeHRX · Traditional | 07/14/1995SE |
| K945390 | Citation Delta ScopeHRX · Traditional | 06/23/1995SE |
| K946290 | Citation Power ToolHRX · Traditional | 06/15/1995SE |
| K951249 | Citation SinuscopeEOB · Traditional | 04/10/1995SE |
| K944976 | Bronchoscope,Non-RigidEOQ · Traditional | 12/21/1994SE |
| K940847 | Endoscopic Plantar Fascia KitHRX · Traditional | 10/11/1994SE |
| K924494 | Citscope, Bendable -- ModificationHRX · Traditional | 05/26/1993SN |
| K922144 | Citscope (Model Extensions)HRX · Traditional | 08/05/1992SE |
| K921692 | Integrated Video SystemHRX · Traditional | 07/01/1992SE |
| K912490 | Citation Medical Scope Procedure PackKKX · Traditional | 08/16/1991SE |
Questions and answers
When was The Biopsy Tool cleared by the FDA?
The Biopsy Tool (K941563) received a 510(k) decision of Substantially Equivalent on September 26, 1994, 178 days after the submission was received.
What is the product code of K941563?
The FDA product code is FCG – Biopsy Needle, a Class II (moderate risk) device regulated under 21 CFR 876.1075.