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NEOLUS NEEDLE

Page Type
Cleared 510(K)
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)
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