510(k) K803301

CREATINE KINASE REAGENT by Gilford Diagnostics — Product Code CGS

K803301 is an FDA 510(k) premarket notification submitted by Gilford Diagnostics for the device "CREATINE KINASE REAGENT". The FDA issued a decision of Substantially Equivalent on January 16, 1981. The device falls under product code CGS (Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes), a Class II device regulated under 21 CFR 862.1215. Gilford Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 16, 1981
Date Received
December 30, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes
Device Class
Class II
Regulation Number
862.1215
Review Panel
CH
Submission Type