510(k) K050784

NICHOLS ADVANTAGE ALDOSTERONE ASSAY by Nichols Institute Diagnostics — Product Code CJM

K050784 is an FDA 510(k) premarket notification submitted by Nichols Institute Diagnostics for the device "NICHOLS ADVANTAGE ALDOSTERONE ASSAY". The FDA issued a decision of Substantially Equivalent on June 1, 2005. The device falls under product code CJM (Radioimmunoassay, Aldosterone), a Class II device regulated under 21 CFR 862.1045. Nichols Institute Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 1, 2005
Date Received
March 28, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Radioimmunoassay, Aldosterone
Device Class
Class II
Regulation Number
862.1045
Review Panel
CH
Submission Type