510(k) K983280

VANCOMYCIN EIA ASSAY by Diagnostic Reagents, Inc. — Product Code LEH

K983280 is an FDA 510(k) premarket notification submitted by Diagnostic Reagents, Inc. for the device "VANCOMYCIN EIA ASSAY". The FDA issued a decision of Substantially Equivalent on November 6, 1998. The device falls under product code LEH (Radioimmunoassay, Vancomycin), a Class II device regulated under 21 CFR 862.3950. Diagnostic Reagents, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 6, 1998
Date Received
September 18, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Vancomycin
Device Class
Class II
Regulation Number
862.3950
Review Panel
TX
Submission Type