Nicore Model NCP-1 External Counterpulsation Device
FDA 510(k) K023016 · Nicore Equipment & Leasing, Inc.
510(k) numberK023016
Submission
- Device name
- Nicore Model NCP-1 External Counterpulsation Device
- Applicant
- Nicore Equipment & Leasing, Inc.
Tampa, FL, US - Received
- September 10, 2002
- Decision date
- December 4, 2002
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DRN – Device, Counter-Pulsating, External
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.5225
- Specialty
- Cardiovascular
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| K250756 | Pression Wave PRO External Counter-Pulsation SystemDRN · Traditional | Pression, Inc. | 12/22/2025SE |
| K202108 | External Counterpulsation System, SoulaireDRN · Special | Vamed Medical Instrument Co., Ltd. | 08/28/2020SE |
| K191955 | Enhanced External Counter Pulsation Device Plus Omay-ADRN · Traditional | Omay(Guangzhou)Med Technologies Co., Ltd. | 08/05/2020SE |
| K190683 | External Counterpulsation SystemDRN · Traditional | Vamed Medical Instrument Co., Ltd. | 09/10/2019SE |
| K173483 | Pure Flow External Counter-Pulsation DeviceDRN · Traditional | Xtreem Pulse, LLC | 05/30/2018SE |
| K152115 | Renew NCP-5 External Counterpulsation SystemDRN · Traditional | Stage 2 Innovations | 12/17/2015SE |
| K130439 | External Counterpulsation Device with SP02 MornitoringDRN · Traditional | Chongqing Psk Sci-Tech Development Co., Ltd. | 12/12/2013SE |
| K082134 | Circulator BootDRN · Traditional | Circulator Boot Corp. | 05/07/2009SE |
| K081359 | Genesis EcpDRN · Special | Scottcare Corporation | 05/29/2008SE |
| K052611 | Ecp Health System, Model 2005DRN · Traditional | Ecp Health, Inc. | 04/26/2006SE |
More from Ecp Health, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K980937 | Nicore Model Esp -1DRN · Traditional | 09/15/2000SE |
Questions and answers
When was Nicore Model NCP-1 External Counterpulsation Device cleared by the FDA?
Nicore Model NCP-1 External Counterpulsation Device (K023016) received a 510(k) decision of Substantially Equivalent on December 4, 2002, 85 days after the submission was received.
What is the product code of K023016?
The FDA product code is DRN – Device, Counter-Pulsating, External, a Class II (moderate risk) device regulated under 21 CFR 870.5225.