510(k) K925998

ACTIVE RENIN IMMUNORADIOMETRIC ASSAY by Nichols Institute Diagnostics — Product Code CIB

K925998 is an FDA 510(k) premarket notification submitted by Nichols Institute Diagnostics for the device "ACTIVE RENIN IMMUNORADIOMETRIC ASSAY". The FDA issued a decision of Substantially Equivalent on January 6, 1993. The device falls under product code CIB (Radioimmunoassay, Angiotensin I And Renin), a Class II device regulated under 21 CFR 862.1085. Nichols Institute Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 6, 1993
Date Received
November 27, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Angiotensin I And Renin
Device Class
Class II
Regulation Number
862.1085
Review Panel
CH
Submission Type