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SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE

Page Type
Cleared 510(K)
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)
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