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MESH FENESTRATED INTRODUCER NEEDLE (MESH INTRODUCER NEEDLE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071375
510(k) Type
Traditional
Applicant
DISC-O-TECH MEDICAL TECHNOLOGIES, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2007
Days to Decision
219 days
Submission Type
Summary

MESH FENESTRATED INTRODUCER NEEDLE (MESH INTRODUCER NEEDLE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071375
510(k) Type
Traditional
Applicant
DISC-O-TECH MEDICAL TECHNOLOGIES, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2007
Days to Decision
219 days
Submission Type
Summary