510(k) K945961

CALCITONIN IMMUNOASSAY KIT by Nichols Institute Diagnostics — Product Code JKR

K945961 is an FDA 510(k) premarket notification submitted by Nichols Institute Diagnostics for the device "CALCITONIN IMMUNOASSAY KIT". The FDA issued a decision of Substantially Equivalent on November 20, 1995. The device falls under product code JKR (Radioimmunoassay, Calcitonin), a Class II device regulated under 21 CFR 862.1140. Nichols Institute Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 20, 1995
Date Received
December 7, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Calcitonin
Device Class
Class II
Regulation Number
862.1140
Review Panel
CH
Submission Type