Last synced on 14 November 2025 at 11:06 pm

GLUCOCARD X-METER BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063771
510(k) Type
Traditional
Applicant
ARKRAY Factory USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2007
Days to Decision
231 days
Submission Type
Summary

GLUCOCARD X-METER BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063771
510(k) Type
Traditional
Applicant
ARKRAY Factory USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2007
Days to Decision
231 days
Submission Type
Summary