Bard Snare Retrieval Kit
FDA 510(k) K152560 · Neometrics, Inc.
510(k) numberK152560
Submission
- Device name
- Bard Snare Retrieval Kit
- Applicant
- Neometrics, Inc.
Plymouth, MN, US - Received
- September 9, 2015
- Decision date
- October 23, 2015
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MMX – Device, Percutaneous Retrieval
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.5150
- Specialty
- Cardiovascular
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| K241259 | Amplatz Goose Neck Snare KitMMX · Special | Medtronic, Inc. | 06/03/2024SE |
| K232443 | Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval KitMMX · Special | Argon Medical Devices, Inc. | 09/07/2023SE |
| K222254 | Gunther Tulip Vena Cava Filter Retrieval SetMMX · Traditional | Cook Incorporated | 05/16/2023SE |
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| K213494 | Aveir Retrieval CatheterMMX · Traditional | Abbott Medical | 04/01/2022SE |
| K200963 | Halo Single-Loop Microsnare KitMMX · Traditional | Argon Medical Devices, Inc. | 01/05/2021SE |
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Questions and answers
When was Bard Snare Retrieval Kit cleared by the FDA?
Bard Snare Retrieval Kit (K152560) received a 510(k) decision of Substantially Equivalent on October 23, 2015, 44 days after the submission was received.
What is the product code of K152560?
The FDA product code is MMX – Device, Percutaneous Retrieval, a Class II (moderate risk) device regulated under 21 CFR 870.5150.