510(k) K955569

INNOFLUOR GENTAMICIN ASSAY SYSTEM by Oxis Intl., Inc. — Product Code LCQ

K955569 is an FDA 510(k) premarket notification submitted by Oxis Intl., Inc. for the device "INNOFLUOR GENTAMICIN ASSAY SYSTEM". The FDA issued a decision of Substantially Equivalent on February 9, 1996. The device falls under product code LCQ (Fluorescent Immunoassay Gentamicin), a Class II device regulated under 21 CFR 862.3450. Oxis Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 9, 1996
Date Received
December 6, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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