Progreat
FDA 510(k) K170223 · Ashitaka Factory of Terumo Corporation
510(k) numberK170223
Submission
- Device name
- Progreat
- Applicant
- Ashitaka Factory of Terumo Corporation
Fujinomiya, JP - Received
- January 25, 2017
- Decision date
- July 21, 2017
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DQO – Catheter, Intravascular, Diagnostic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1200
- Specialty
- Cardiovascular
Other 510(k)s with product code DQO
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261455 | Arterial Pressure Monitoring Set/TrayDQO · Traditional | Spectrum Vascular | 06/26/2026SE |
| K252702 | Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF…DQO · Traditional | Bioptimal International Pte. , Ltd. | 05/28/2026SE |
| K254278 | Arterial Pressure Monitoring Set/TrayDQO · Special | Spectrum Vascular | 03/25/2026SE |
| K250751 | DualView CatheterDQO · Traditional | Terumo Corporation | 07/17/2025SE |
| K242966 | Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterDQO · Traditional | Gentuity, LLC | 01/31/2025SE |
| K242420 | pNOVUS 21 MicrocatheterDQO · Traditional | Phenox, Ltd. | 11/12/2024SE |
| K233268 | Impress Angiographic CatheterDQO · Special | Merit Medical Systems, Inc. | 05/22/2024SE |
| K233975 | Zoom 6F Insert CathetersDQO · Traditional | Imperative Care, Inc. | 04/02/2024SE |
| K232536 | Soldier MicrocatheterDQO · Traditional | Embolx, Inc. | 02/23/2024SE |
| K232573 | INFINITI Ambi Angiographic CatheterDQO · Traditional | Cordis US Corp | 11/21/2023SE |
More from Cordis US Corp
| 510(k) | Device | Decision |
|---|---|---|
| K203521 | FineCross M3DQY · Traditional | 03/03/2021SE |
| K161546 | R2P SlenGuideDQY · Traditional | 10/14/2016SE |
| K152740 | Radifocus GlidewireDQX · Traditional | 11/16/2015SE |
| K150232 | Radifocus Optitorque Angiographic CatheterDQO · Traditional | 10/19/2015SE |
| K130520 | Capiox FX15 and FX25 Hollow Fiber Oxygenator/ReservoirDTZ · Special | 03/13/2013SE |
Questions and answers
When was Progreat cleared by the FDA?
Progreat (K170223) received a 510(k) decision of Substantially Equivalent on July 21, 2017, 177 days after the submission was received.
What is the product code of K170223?
The FDA product code is DQO – Catheter, Intravascular, Diagnostic, a Class II (moderate risk) device regulated under 21 CFR 870.1200.