FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
FFRct
K Number: K182035
·
Decision Dec 6, 2018
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
8
Applicant Total
7
Review Days
129
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Basic Information
- Device Name
- FFRct
- K Number
- K182035
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.1415
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- HeartFlow, Inc.
- Date Received
- July 30, 2018
- Decision Date
- December 6, 2018
- Product Code
- PJA
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| PJA | Coronary Vascular Physiologic Simulation Software | FDA class 2 | Cardiovascular |
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Other Clearances by HeartFlow, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K250902 | HeartFlow Analysis | Jul 18, 2025 | Substantially Equivalent |
| K213857 | HeartFlow Analysis | Oct 14, 2022 | Substantially Equivalent |
| K203329 | HeartFlow Analysis | Jan 8, 2021 | Substantially Equivalent |
| K190925 | HeartFlow FFRct Analysis | Aug 15, 2019 | Substantially Equivalent |
| K161772 | FFRct | Aug 24, 2016 | Substantially Equivalent |
| K152733 | FFRct | Jan 13, 2016 | Substantially Equivalent |