510(k) K960053

SELFCARE BLOOD GLUCOSE TEST STRIPS FOR THE EXACTECH SYSTEM by Selfcare, Inc. — Product Code CGA

K960053 is an FDA 510(k) premarket notification submitted by Selfcare, Inc. for the device "SELFCARE BLOOD GLUCOSE TEST STRIPS FOR THE EXACTECH SYSTEM". The FDA issued a decision of Substantially Equivalent on June 28, 1996. The device falls under product code CGA (Glucose Oxidase, Glucose), a Class II device regulated under 21 CFR 862.1345. Selfcare, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 28, 1996
Date Received
January 4, 1996
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