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TEMPORARY SCREENING LEAD/CATHETER KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934938
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1994
Days to Decision
239 days
Submission Type
Summary

TEMPORARY SCREENING LEAD/CATHETER KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934938
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1994
Days to Decision
239 days
Submission Type
Summary