The Caterpillar and Caterpillar Micro Arterial Embolization Devices
FDA 510(k) K191532 · C.R. Bard, Inc.
510(k) numberK191532
Submission
- Device name
- The Caterpillar and Caterpillar Micro Arterial Embolization Devices
- Applicant
- C.R. Bard, Inc.
Enniscorthy, IE - Received
- June 10, 2019
- Decision date
- February 4, 2020
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KRD – Device, Vascular, For Promoting Embolization
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.3300
- Specialty
- Cardiovascular
- Implant
- Yes
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|---|---|---|---|
| K252812 | UniPearls® Embolic MicrospheresKRD · Traditional | Suzhou Haowei Medical Technology Co., Ltd. | 07/31/2026SE |
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| K260508 | LOBO Vascular Occlusion SystemKRD · Traditional | Okami Medical, Inc. | 04/10/2026SE |
| K253511 | Concerto Versa Detachable CoilKRD · Traditional | Medtronic, Inc. | 01/14/2026SE |
| K253677 | Tembo Embolic SystemKRD · Special | Instylla, Inc. | 12/15/2025SE |
| K253376 | OBSIDIO Conformable Embolic (M0013972101010)KRD · Special | Boston Scientific Corporation | 10/30/2025SE |
| K250209 | Polyvinyl Alcohol Embolic MicrospheresKRD · Traditional | Canyon Medical, Inc. | 09/23/2025SE |
| K250133 | HARBOR Occlusion DeviceKRD · Traditional | Nuvascular, Inc. | 07/09/2025SE |
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Questions and answers
When was The Caterpillar and Caterpillar Micro Arterial Embolization Devices cleared by the FDA?
The Caterpillar and Caterpillar Micro Arterial Embolization Devices (K191532) received a 510(k) decision of Substantially Equivalent on February 4, 2020, 239 days after the submission was received.
What is the product code of K191532?
The FDA product code is KRD – Device, Vascular, For Promoting Embolization, a Class II (moderate risk) device regulated under 21 CFR 870.3300.