510(k) K915465

DIGITOXIN FPIA REAGENT SET by Sigma Diagnostics, Inc. — Product Code LFM

K915465 is an FDA 510(k) premarket notification submitted by Sigma Diagnostics, Inc. for the device "DIGITOXIN FPIA REAGENT SET". The FDA issued a decision of Substantially Equivalent on January 27, 1992. The device falls under product code LFM (Enzyme Immunoassay, Digitoxin), a Class II device regulated under 21 CFR 862.3300. Sigma Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 27, 1992
Date Received
December 2, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Digitoxin
Device Class
Class II
Regulation Number
862.3300
Review Panel
TX
Submission Type