Last synced on 23 May 2025 at 11:06 pm

SURESTEP BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984261
510(k) Type
Traditional
Applicant
LIFESCAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1999
Days to Decision
175 days
Submission Type
Summary

SURESTEP BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984261
510(k) Type
Traditional
Applicant
LIFESCAN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1999
Days to Decision
175 days
Submission Type
Summary