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SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130843
510(k) Type
Traditional
Applicant
Oscor, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2014
Days to Decision
287 days
Submission Type
Statement

SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130843
510(k) Type
Traditional
Applicant
Oscor, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2014
Days to Decision
287 days
Submission Type
Statement