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NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 40053, 40042 & 40013

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031173
510(k) Type
Traditional
Applicant
NEEDLETECH PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2003
Days to Decision
100 days
Submission Type
Summary

NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 40053, 40042 & 40013

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031173
510(k) Type
Traditional
Applicant
NEEDLETECH PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2003
Days to Decision
100 days
Submission Type
Summary