510(k) K897072

NDS THYROXINE TEST KIT & NDS THYROXINE CALIBRATOR by Kallestad Diag, A Div. of Erbamont, Inc. — Product Code KLI

K897072 is an FDA 510(k) premarket notification submitted by Kallestad Diag, A Div. of Erbamont, Inc. for the device "NDS THYROXINE TEST KIT & NDS THYROXINE CALIBRATOR". The FDA issued a decision of Substantially Equivalent on March 29, 1990. The device falls under product code KLI (Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine), a Class II device regulated under 21 CFR 862.1700. Kallestad Diag, A Div. of Erbamont, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 29, 1990
Date Received
December 22, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine
Device Class
Class II
Regulation Number
862.1700
Review Panel
CH
Submission Type