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DROPLET PEN NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171982
510(k) Type
Traditional
Applicant
HTL-STREFA S.A.
Country
Poland
FDA Decision
Substantially Equivalent
Decision Date
3/21/2018
Days to Decision
264 days
Submission Type
Summary

DROPLET PEN NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171982
510(k) Type
Traditional
Applicant
HTL-STREFA S.A.
Country
Poland
FDA Decision
Substantially Equivalent
Decision Date
3/21/2018
Days to Decision
264 days
Submission Type
Summary