510(k) K863102

GLUCOMETER-E by J. D. Assoc. — Product Code CGA

K863102 is an FDA 510(k) premarket notification submitted by J. D. Assoc. for the device "GLUCOMETER-E". The FDA issued a decision of Substantially Equivalent on November 24, 1986. The device falls under product code CGA (Glucose Oxidase, Glucose), a Class II device regulated under 21 CFR 862.1345. J. D. Assoc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 24, 1986
Date Received
August 13, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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