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VERRES NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K932281
510(k) Type
Traditional
Applicant
SURGEON SURGICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/1993
Days to Decision
86 days
Submission Type
Statement

VERRES NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K932281
510(k) Type
Traditional
Applicant
SURGEON SURGICAL INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/1993
Days to Decision
86 days
Submission Type
Statement