| Device Type ID | 440 |
| Device Name | Nitroprusside, Ketones (urinary, Non-quant.) |
| Regulation Description | Ketones (nonquantitative) Test System. |
| Regulation Medical Specialty | Clinical Chemistry |
| Review Panel | Clinical Chemistry |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 862.1435 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | JIN |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
|
| Device Type ID | 440 |
| Device | Nitroprusside, Ketones (urinary, Non-quant.) |
| Product Code | JIN |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Ketones (nonquantitative) Test System. |
| CFR Regulation Number | 862.1435 [🔎] |
| Premarket Reviews | ||
|---|---|---|
| Manufacturer | Decision | |
ACON LABORATORIES, INC. | ||
SUBSTANTIALLY EQUIVALENT | 1 | |
APEX BIOTECHNOLOGY CORP. | ||
SUBSTANTIALLY EQUIVALENT | 1 | |
I-SENS, INC. | ||
SUBSTANTIALLY EQUIVALENT | 1 | |
TAIDOC TECHNOLOGY CORPORATION | ||
SUBSTANTIALLY EQUIVALENT | 1 | |
| Device Problems | |
|---|---|
Appropriate Term/Code Not Available | 1 |
| Total Device Problems | 1 |