510(k) K962519

EMIT 2000 GENTAMICIN ASSAY AND CALIBRATORS by Behring Diagnostics, Inc. — Product Code LCD

K962519 is an FDA 510(k) premarket notification submitted by Behring Diagnostics, Inc. for the device "EMIT 2000 GENTAMICIN ASSAY AND CALIBRATORS". The FDA issued a decision of Substantially Equivalent on September 4, 1996. The device falls under product code LCD (Enzyme Immunoassay, Gentamicin), a Class II device regulated under 21 CFR 862.3450. Behring Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 4, 1996
Date Received
June 27, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Immunoassay, Gentamicin
Device Class
Class II
Regulation Number
862.3450
Review Panel
TX
Submission Type