510(k) K042329

SALICYLATE-SL ASSAY by Diagnostic Chemicals , Ltd. — Product Code DKJ

K042329 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals , Ltd. for the device "SALICYLATE-SL ASSAY". The FDA issued a decision of Substantially Equivalent on December 27, 2004. The device falls under product code DKJ (Colorimetry, Salicylate), a Class II device regulated under 21 CFR 862.3830. Diagnostic Chemicals , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 27, 2004
Date Received
August 27, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimetry, Salicylate
Device Class
Class II
Regulation Number
862.3830
Review Panel
TX
Submission Type