510(k) K993920

ETHANOL-L3K ASSAY, CATALOGUE NUMBER 273-30, 273-17 by Diagnostic Chemicals , Ltd. — Product Code DIC

K993920 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals , Ltd. for the device "ETHANOL-L3K ASSAY, CATALOGUE NUMBER 273-30, 273-17". The FDA issued a decision of Substantially Equivalent on January 18, 2000. The device falls under product code DIC (Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method), a Class II device regulated under 21 CFR 862.3040. Diagnostic Chemicals , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 18, 2000
Date Received
November 18, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method
Device Class
Class II
Regulation Number
862.3040
Review Panel
TX
Submission Type