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 |