510(k) K050419

QMS VANCOMYCIN by Seradyn, Inc. — Product Code LEH

K050419 is an FDA 510(k) premarket notification submitted by Seradyn, Inc. for the device "QMS VANCOMYCIN". The FDA issued a decision of Substantially Equivalent on April 1, 2005. The device falls under product code LEH (Radioimmunoassay, Vancomycin), a Class II device regulated under 21 CFR 862.3950. Seradyn, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 1, 2005
Date Received
February 18, 2005
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