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29G AND 30G K-PACK II NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K062608
510(k) Type
Special
Applicant
TERUMO EUROPE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
9/15/2006
Days to Decision
10 days
Submission Type
Summary

29G AND 30G K-PACK II NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K062608
510(k) Type
Special
Applicant
TERUMO EUROPE N.V.
Country
Belgium
FDA Decision
Substantially Equivalent
Decision Date
9/15/2006
Days to Decision
10 days
Submission Type
Summary