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MICROSURGE VERESS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K954520
510(k) Type
Traditional
Applicant
MICROSURGE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1995
Days to Decision
18 days
Submission Type
Summary

MICROSURGE VERESS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K954520
510(k) Type
Traditional
Applicant
MICROSURGE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1995
Days to Decision
18 days
Submission Type
Summary