L-F Coiled Extension Tubing
FDA 510(k) K882329 · Mallinckrodt Group, Inc.
510(k) numberK882329
Submission
- Device name
- L-F Coiled Extension Tubing
- Applicant
- Mallinckrodt Group, Inc.
Cincinnati, OH, US - Received
- June 6, 1988
- Decision date
- September 2, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DXT – Injector And Syringe, Angiographic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1650
- Specialty
- Cardiovascular
Other 510(k)s with product code DXT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252652 | Disposable Syringes with Accessories for Power Injectors (900103T); Disposable Syringes…DXT · Traditional | Fortis Biosolutions Company Limited | 05/14/2026SE |
| K252653 | ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module…DXT · Traditional | Acist Medical Systems, Inc. | 05/13/2026SE |
| K252638 | VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use…DXT · Traditional | Acist Medical Systems, Inc. | 05/13/2026SE |
| K253048 | High Pressure Syringe; Pressure Connecting Tube; Quick fill tube; Spike; Transfer TubeDXT · Traditional | Shenzhen Maiwei Biotech Co., Ltd. | 04/16/2026SE |
| K251788 | Extension tubeDXT · Traditional | Zhuhai DR Medical Instruments Co., Ltd. | 03/05/2026SE |
| K252891 | MEDRAD MRXperion MR Injection System and MR Injection System Syringe Kit; MEDRAD ISI2…DXT · Traditional | Bayer Medical Care, Inc. | 02/13/2026SE |
| K244038 | High Pressure TubingDXT · Traditional | Shandong Int Medical Instruments Co., Ltd. | 09/05/2025SE |
| K242143 | Angiography InjectorDXT · Traditional | Shandong Int Medical Instruments Co., Ltd. | 12/23/2024SE |
| K242212 | Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)DXT · Traditional | Nemoto Kyorindo Co., Ltd. | 08/27/2024SE |
| K241109 | Single-use Sterile High-pressure Angiographic Syringes and AccessoriesDXT · Traditional | Shenzhen Boon Medical Supply Co., Ltd. | 08/22/2024SE |
More from Shenzhen Boon Medical Supply Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K945053 | LF CT Hig Pressure CathetersFOZ · Traditional | 05/19/1995SE |
| K945140 | Uro-FloLJH · Traditional | 03/08/1995SE |
| K943581 | Hydradjust IV Urological TableIXR · Traditional | 01/04/1995SE |
| K943122 | Surgical DrapesKKX · Traditional | 09/07/1994SE |
| K934664 | HydragownFYA · Traditional | 05/24/1994SE |
| K920742 | Hydrajust IV Urological TableIXR · Traditional | 04/27/1992SE |
| K912944 | CT 8000 Digital Injection SystemDXT · Traditional | 02/04/1992SE |
| K913264 | Hydraview 1000 Digital Image Process/Stor DeviceLLZ · Traditional | 11/01/1991SE |
| K905789 | Franklin 9000 Wall StandKPX · Traditional | 05/20/1991SE |
| K904147 | Hugh Young II Urological X-Ray SystemKPR · Traditional | 12/13/1990SE |
Questions and answers
When was L-F Coiled Extension Tubing cleared by the FDA?
L-F Coiled Extension Tubing (K882329) received a 510(k) decision of Substantially Equivalent on September 2, 1988, 88 days after the submission was received.
What is the product code of K882329?
The FDA product code is DXT – Injector And Syringe, Angiographic, a Class II (moderate risk) device regulated under 21 CFR 870.1650.