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NovoPen Echo Dial-A-Dose Insulin Delivery Device (Pen Injector)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182387
510(k) Type
Traditional
Applicant
Novo Nordisk, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2018
Days to Decision
104 days
Submission Type
Summary

NovoPen Echo Dial-A-Dose Insulin Delivery Device (Pen Injector)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182387
510(k) Type
Traditional
Applicant
Novo Nordisk, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2018
Days to Decision
104 days
Submission Type
Summary