510(k) K070383

ENZYMATIC CREATININE ASSAY (265 SERIES) by Diagnostic Chemicals , Ltd. — Product Code JFY

K070383 is an FDA 510(k) premarket notification submitted by Diagnostic Chemicals , Ltd. for the device "ENZYMATIC CREATININE ASSAY (265 SERIES)". The FDA issued a decision of Substantially Equivalent on June 22, 2007. The device falls under product code JFY (Enzymatic Method, Creatinine), a Class II device regulated under 21 CFR 862.1225. Diagnostic Chemicals , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 22, 2007
Date Received
February 9, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzymatic Method, Creatinine
Device Class
Class II
Regulation Number
862.1225
Review Panel
CH
Submission Type