510(k) K861311

GLUCOSE (HEXOKINASE) REAGENT SET by Sterling Diagnostics, Inc. — Product Code CFR

K861311 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "GLUCOSE (HEXOKINASE) REAGENT SET". The FDA issued a decision of Substantially Equivalent on April 24, 1986. The device falls under product code CFR (Hexokinase, Glucose), a Class II device regulated under 21 CFR 862.1345. Sterling Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 24, 1986
Date Received
April 8, 1986
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