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DUAL LUMEN EMBOLECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K970762
510(k) Type
Traditional
Applicant
Applied Medical Resources
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1997
Days to Decision
25 days
Submission Type
Summary

DUAL LUMEN EMBOLECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K970762
510(k) Type
Traditional
Applicant
Applied Medical Resources
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1997
Days to Decision
25 days
Submission Type
Summary