Vascular Access Cath. Repair Kit
FDA 510(k) K833915 · Cormed, Inc., Sub. C.R.Bard, Inc.
510(k) numberK833915
Submission
- Device name
- Vascular Access Cath. Repair Kit
- Applicant
- Cormed, Inc., Sub. C.R.Bard, Inc.
Mchenry, IL, US - Received
- November 14, 1983
- Decision date
- March 30, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- LJS – Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5970
- Specialty
- General Hospital
- Implant
- Yes
Other 510(k)s with product code LJS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260929 | Neonav ECG Tip Location SystemLJS · Special | Navi Medical Technologies | 04/17/2026SE |
| K252373 | BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with…LJS · Traditional | Spectrum Vascular | 12/16/2025SE |
| K252792 | PM2 System with ECGuide ConnectorLJS · Special | Piccolo Medical, Inc. | 11/17/2025SE |
| K243458 | HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301)…LJS · Traditional | Access Vascular, Inc. | 08/01/2025SE |
| K251212 | Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC…LJS · Special | Access Vascular, Inc. | 07/01/2025SE |
| K243484 | PM2+ System and SmartPICC StyletLJS · Traditional | Piccolo Medical, Inc. | 05/29/2025SE |
| K241587 | pilot TLSLJS · Traditional | Vygon Corporation | 02/26/2025SE |
| K241910 | Neonav ECG Tip Location SystemLJS · Traditional | Navi Medical Technologies | 01/19/2025SE |
| K243941 | HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001201)…LJS · Special | Access Vascular, Inc. | 01/17/2025SE |
| K240486 | PM2 System and ECGuide ConnectorLJS · Traditional | Piccolo Medical, Inc. | 09/08/2024SE |
More from Piccolo Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K863606 | Butterfly Non-Coring Needle SetFMI · Traditional | 12/18/1986SE |
| K860432 | Percutaneous Introducer KitDYB · Traditional | 03/31/1986SE |
| K854019 | Port-GardLJT · Traditional | 11/26/1985SE |
| K850967 | Sterile Cormed MediportLJT · Traditional | 05/17/1985SE |
| K850674 | Cormed II Ambulatory Infusion PumpFRN · Traditional | 04/09/1985SE |
| K843083 | Cormed Huber Point NeedleGAA · Traditional | 09/05/1984SE |
| K823553 | Corcath H & B Vascular Access CatheterLJS · Traditional | 01/05/1983SE |
Questions and answers
When was Vascular Access Cath. Repair Kit cleared by the FDA?
Vascular Access Cath. Repair Kit (K833915) received a 510(k) decision of Substantially Equivalent on March 30, 1984, 137 days after the submission was received.
What is the product code of K833915?
The FDA product code is LJS – Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days, a Class II (moderate risk) device regulated under 21 CFR 880.5970.