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FLEX-NECK ARC CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070730
510(k) Type
Traditional
Applicant
MEDIGROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/3/2007
Days to Decision
110 days
Submission Type
Summary

FLEX-NECK ARC CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070730
510(k) Type
Traditional
Applicant
MEDIGROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
7/3/2007
Days to Decision
110 days
Submission Type
Summary