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FLEXPEN NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K090111
510(k) Type
Traditional
Applicant
NOVO NORDISK INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2010
Days to Decision
381 days
Submission Type
Summary

FLEXPEN NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K090111
510(k) Type
Traditional
Applicant
NOVO NORDISK INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2010
Days to Decision
381 days
Submission Type
Summary