510(k) K860045

DETERMINATION OF GENTAMICIN by Clinical Data, Inc. — Product Code LCD

K860045 is an FDA 510(k) premarket notification submitted by Clinical Data, Inc. for the device "DETERMINATION OF GENTAMICIN". The FDA issued a decision of Substantially Equivalent on January 22, 1986. The device falls under product code LCD (Enzyme Immunoassay, Gentamicin), a Class II device regulated under 21 CFR 862.3450. Clinical Data, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 22, 1986
Date Received
January 6, 1986
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