Radioassay, 17-hydroxycorticosteroids

Device Code: 412

Product Code(s): JHE

Device Classification Information

Device Type ID412
Device NameRadioassay, 17-hydroxycorticosteroids
Regulation Description17-Hydroxycorticosteroids (17-ketogenic Steroids) Test System.
Regulation Medical SpecialtyClinical Chemistry
Review PanelClinical Chemistry
Premarket Review Office Of In Vitro Diagnostics And Radiological Health (OIR)
Submission Type510(K) Exempt
CFR Regulation Number862.1385 [🔎]
FDA Device ClassificationClass 1 Medical Device
Product CodeJHE
GMP ExemptNo
Summary MREligible
Implanted DeviceNo
Life Support DeviceNo
Third Party Review Not Third Party Eligible

Recognized Standards

Total Product Life Cycle

Device Type ID412
DeviceRadioassay, 17-hydroxycorticosteroids
Product CodeJHE
FDA Device ClassificationClass 1 Medical Device
Regulation Description17-Hydroxycorticosteroids (17-ketogenic Steroids) Test System.
CFR Regulation Number862.1385 [🔎]
TPLC Last Update: 2019-04-02 19:34:15

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.