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MODIFICATION TO EVENCARE BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031843
510(k) Type
Special
Applicant
Medline Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2003
Days to Decision
17 days
Submission Type
Statement

MODIFICATION TO EVENCARE BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031843
510(k) Type
Special
Applicant
Medline Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/2003
Days to Decision
17 days
Submission Type
Statement