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ACCU-CHEK ULTRFLEX INFUSION SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101196
510(k) Type
Special
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2010
Days to Decision
120 days
Submission Type
Summary

ACCU-CHEK ULTRFLEX INFUSION SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101196
510(k) Type
Special
Applicant
ROCHE DIAGNOSTICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2010
Days to Decision
120 days
Submission Type
Summary