510(k) K874223

EMIT TOBRAMYCIN ASSAY by Syva Co. — Product Code KLB

K874223 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "EMIT TOBRAMYCIN ASSAY". The FDA issued a decision of Substantially Equivalent on November 13, 1987. The device falls under product code KLB (Radioimmunoassay, Tobramycin), a Class II device regulated under 21 CFR 862.3900. Syva Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 13, 1987
Date Received
October 16, 1987
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