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K-PACK II NEEDLE - 29G THIN WALL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082820
510(k) Type
Special
Applicant
TERUMO EUROPE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
10/23/2008
Days to Decision
28 days
Submission Type
Summary

K-PACK II NEEDLE - 29G THIN WALL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082820
510(k) Type
Special
Applicant
TERUMO EUROPE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
10/23/2008
Days to Decision
28 days
Submission Type
Summary