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NEOLUS NEEDLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001572
510(k) Type
Traditional
Applicant
Terumo Europe N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
8/14/2000
Days to Decision
84 days
Submission Type
Summary

NEOLUS NEEDLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001572
510(k) Type
Traditional
Applicant
Terumo Europe N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
8/14/2000
Days to Decision
84 days
Submission Type
Summary