510(k) K050784
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