510(k) K811849

ESKAFLOW TEST FOR GLUCOSE by Smithkline Diagnostics, Inc. — Product Code CFR

K811849 is an FDA 510(k) premarket notification submitted by Smithkline Diagnostics, Inc. for the device "ESKAFLOW TEST FOR GLUCOSE". The FDA issued a decision of Substantially Equivalent on July 15, 1981. The device falls under product code CFR (Hexokinase, Glucose), a Class II device regulated under 21 CFR 862.1345. Smithkline Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 15, 1981
Date Received
July 1, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hexokinase, Glucose
Device Class
Class II
Regulation Number
862.1345
Review Panel
CH
Submission Type