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COHERENT SLIMLINE SINGLE LUMEN ASPIRATION NEEDLE KIT

Page Type
Cleared 510(K)
510(k) Number
K960413
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1996
Days to Decision
66 days
Submission Type
Summary

COHERENT SLIMLINE SINGLE LUMEN ASPIRATION NEEDLE KIT

Page Type
Cleared 510(K)
510(k) Number
K960413
510(k) Type
Traditional
Applicant
LUMENIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1996
Days to Decision
66 days
Submission Type
Summary