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ANGIOJET XPEEDIOR 120 CATHETER AND ANGIOJET POWER PULSE SPRAY ANCILLARY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040013
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2004
Days to Decision
134 days
Submission Type
Summary

ANGIOJET XPEEDIOR 120 CATHETER AND ANGIOJET POWER PULSE SPRAY ANCILLARY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040013
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2004
Days to Decision
134 days
Submission Type
Summary