FDA 510(k)
FDA class 2
Substantially Equivalent
🇦🇺 Australia
SOZO Pro
K Number: K232089
·
Decision Oct 17, 2023
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
113
Applicant Total
12
Review Days
96
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Basic Information
- Device Name
- SOZO Pro
- K Number
- K232089
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2770
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- ImpediMed Limited
- Date Received
- July 13, 2023
- Decision Date
- October 17, 2023
- Product Code
- DSB
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| DSB | Plethysmograph, Impedance | FDA class 2 | Cardiovascular |
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Other Clearances by ImpediMed Limited
| K Number | Device Name | ||
|---|---|---|---|
| K253224 | MySOZO Software version 6.0.1.2 (SW version 6.0.1.2) | Jan 28, 2026 | Substantially Equivalent |
| K230530 | SOZO Pro | May 4, 2023 | Substantially Equivalent |
| K230531 | SOZO Pro | May 4, 2023 | Substantially Equivalent |
| K203473 | SOZO | Apr 19, 2021 | Substantially Equivalent |
| K193410 | SOZO Body Fluid Analyzer | Oct 2, 2020 | Substantially Equivalent |
| K190529 | SOZO | Nov 25, 2019 | Substantially Equivalent |
| K180126 | SOZO | Apr 16, 2018 | Substantially Equivalent |
| K172507 | SOZO | Dec 22, 2017 | Substantially Equivalent |
| K172122 | SOZO | Aug 11, 2017 | Substantially Equivalent |
| K130338 | IMPEDIMED - BIS EXTRA CELLULAR FLUID ANALYSIS | May 31, 2013 | Substantially Equivalent |