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K-Pack Enhance Needle (KH-2713RBBTC and KH-2913RBBTC)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243581
510(k) Type
Traditional
Applicant
Terumo Europe N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
4/4/2025
Days to Decision
141 days
Submission Type
Summary

K-Pack Enhance Needle (KH-2713RBBTC and KH-2913RBBTC)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243581
510(k) Type
Traditional
Applicant
Terumo Europe N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
4/4/2025
Days to Decision
141 days
Submission Type
Summary