510(k) K962819

GENTAMICIN FLEX REAGENT CARTRIDGE by Dade Intl., Inc. — Product Code LCD

K962819 is an FDA 510(k) premarket notification submitted by Dade Intl., Inc. for the device "GENTAMICIN FLEX REAGENT CARTRIDGE". The FDA issued a decision of Substantially Equivalent on September 13, 1996. The device falls under product code LCD (Enzyme Immunoassay, Gentamicin), a Class II device regulated under 21 CFR 862.3450. Dade Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 13, 1996
Date Received
July 19, 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