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PRECISION XTRA ADVANCED DIABETES MANAGEMENT SYSTEM, PRECISION BLOOD GLUCOSE TEST STRIPS, PRECISION XTRA B-KETONE TEST ST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983504
510(k) Type
Traditional
Applicant
Medisense, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1999
Days to Decision
276 days
Submission Type
Summary

PRECISION XTRA ADVANCED DIABETES MANAGEMENT SYSTEM, PRECISION BLOOD GLUCOSE TEST STRIPS, PRECISION XTRA B-KETONE TEST ST

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983504
510(k) Type
Traditional
Applicant
Medisense, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1999
Days to Decision
276 days
Submission Type
Summary