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CO-AXIAL INTRODUCER NEEDLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022634
510(k) Type
Traditional
Applicant
Promex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2002
Days to Decision
90 days
Submission Type
Statement

CO-AXIAL INTRODUCER NEEDLE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022634
510(k) Type
Traditional
Applicant
Promex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2002
Days to Decision
90 days
Submission Type
Statement