510(k) K980032

SALICYLATE ASSAY (ACE), CATALOGUE NUMBER 501-71 by Diagnostic Chemicals , Ltd. — Product Code DKJ

K980032 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals , Ltd. for the device "SALICYLATE ASSAY (ACE), CATALOGUE NUMBER 501-71". The FDA issued a decision of Substantially Equivalent on March 2, 1998. 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
March 2, 1998
Date Received
January 5, 1998
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