510(k) K791596

FLUOROMATIC TOBRAMYCIN FIA IMMUNOASSAY by Bio-Rad — Product Code KLB

K791596 is an FDA 510(k) premarket notification submitted by Bio-Rad for the device "FLUOROMATIC TOBRAMYCIN FIA IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on October 17, 1979. The device falls under product code KLB (Radioimmunoassay, Tobramycin), a Class II device regulated under 21 CFR 862.3900. Bio-Rad has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 17, 1979
Date Received
August 15, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Tobramycin
Device Class
Class II
Regulation Number
862.3900
Review Panel
TX
Submission Type