Modification to Temno Biopsy Needles
FDA 510(k) K024120 · Allegiance Healthcare Corp.
510(k) numberK024120
Submission
- Device name
- Modification to Temno Biopsy Needles
- Applicant
- Allegiance Healthcare Corp.
Mcgaw Park, IL, US - Received
- December 16, 2002
- Decision date
- January 15, 2003
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary 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 |
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| K023602 | Small Volume NebulizerCAF · Special | 05/01/2003SE |
| K023419 | Trilaminate Drapes/TiburonKKX · Traditional | 02/11/2003SE |
| K024292 | Modification to Positive Touch Powder-Free Latex Examination Gloves with Protein and…LYY · Special | 01/09/2003SE |
| K024102 | Dental Powder-Free Latex Examination Gloves with Protein Labeling ClaimLYY · Special | 12/18/2002SE |
| K023425 | Drapes with Absorbent ReinforcementKKX · Special | 11/06/2002SE |
| K022765 | Nitrile Powder-Free Examination GlovesLZA · Traditional | 10/11/2002SE |
| K023170 | Nitrile Powder-Free Examination GlovesLZA · Special | 10/09/2002SE |
| K023167 | Breathable Surgical GownFYA · Special | 10/02/2002SE |
| K012931 | Genesis Sterrad Compatible Reusable Sterilization Container SystemFRG · Traditional | 08/20/2002SE |
Questions and answers
When was Modification to Temno Biopsy Needles cleared by the FDA?
Modification to Temno Biopsy Needles (K024120) received a 510(k) decision of Substantially Equivalent on January 15, 2003, 30 days after the submission was received.
What is the product code of K024120?
The FDA product code is FCG – Biopsy Needle, a Class II (moderate risk) device regulated under 21 CFR 876.1075.