510(k) K955570

INNOFLUOR AMIKACIN ASSAY SYSTEM by Oxis Intl., Inc. — Product Code KLQ

K955570 is an FDA 510(k) premarket notification submitted by Oxis Intl., Inc. for the device "INNOFLUOR AMIKACIN ASSAY SYSTEM". The FDA issued a decision of Substantially Equivalent on February 9, 1996. The device falls under product code KLQ (Radioimmunoassay, Amikacin), a Class II device regulated under 21 CFR 862.3035. 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
Radioimmunoassay, Amikacin
Device Class
Class II
Regulation Number
862.3035
Review Panel
TX
Submission Type