JLE · Radioimmunoassay, Desoxycorticosterone
Clinical Chemistry · 21 CFR 862.1250 · Class 1
Overview
| Product Code | JLE |
|---|---|
| Device Name | Radioimmunoassay, Desoxycorticosterone |
| Regulation | 21 CFR 862.1250 |
| Device Class | Class 1 |
| Review Panel | Clinical Chemistry |
Identification
A desoxycorticosterone test system is a device intended to measure desoxycorticosterone (DOC) in plasma and urine. DOC measurements are used in the diagnosis and treatment of patients with hypermineralocorticoidism (excess retention of sodium and loss of potassium) and other disorders of the adrenal gland.
Classification Rationale
Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 862.9.
Recent Cleared Devices (0 of 0)
No cleared devices on record.
