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TROCAR STYLE NEEDLE/CO-AXIAL INTRODUCER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K954265
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1995
Days to Decision
17 days
Submission Type
Statement

TROCAR STYLE NEEDLE/CO-AXIAL INTRODUCER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K954265
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1995
Days to Decision
17 days
Submission Type
Statement