NEPHROCHECK TEST SYSTEM
FDA 510(k) clearance DEN130031 · decided 2014-09-05
Clearance details
- K-number
- DEN130031
- Device name
- NEPHROCHECK TEST SYSTEM
- Applicant
- Astute Medical, Inc.
- Decision
- Unknown
- Date received
- 2013-06-05
- Decision date
- 2014-09-05
- Days to decision
- 457 days
- Clearance type
- Direct
- Product code
- PIG
- Device class
- 2
- Regulation number
- 862.1220
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- San Diego, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| ProNephro AKI™ (NGAL) (K232761) | Bioporto Diagnostic, Inc. | 2023-12-07 |
| VIDAS NEPHROCHECK (K210793) | Biomérieux SA | 2022-07-08 |
| NEPHROCHECK Test System (K171482) | Astute Medical, Inc. | 2017-11-16 |
| NEPHROCHECK Test Kit, ASTUTE140 Meter, NEPHROCHECK Liquid Controls Kit, NEPHROCHECK Calibration Verification (Cal Vers) Kit (K153165) | Astute Medical, Inc. | 2016-06-01 |
Recalls involving this device
No recalls on record reference this clearance.