510(k) K854184

IN-VITRO TEST DETERMINATION OF TOBRAMYCIN by Clinical Data, Inc. — Product Code KLB

K854184 is an FDA 510(k) premarket notification submitted by Clinical Data, Inc. for the device "IN-VITRO TEST DETERMINATION OF TOBRAMYCIN". The FDA issued a decision of Substantially Equivalent on December 4, 1985. The device falls under product code KLB (Radioimmunoassay, Tobramycin), a Class II device regulated under 21 CFR 862.3900. Clinical Data, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 4, 1985
Date Received
October 15, 1985
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