510(k) K900009

NDS THEOPHYLLINE TEST KIT & NDS TDM CALIBRATOR SET by Kallestad Diag, A Div. of Erbamont, Inc. — Product Code KLS

K900009 is an FDA 510(k) premarket notification submitted by Kallestad Diag, A Div. of Erbamont, Inc. for the device "NDS THEOPHYLLINE TEST KIT & NDS TDM CALIBRATOR SET". The FDA issued a decision of Substantially Equivalent on March 29, 1990. The device falls under product code KLS (Enzyme Immunoassay, Theophylline), a Class II device regulated under 21 CFR 862.3880. 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
January 2, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Theophylline
Device Class
Class II
Regulation Number
862.3880
Review Panel
TX
Submission Type