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SINGLE LUMEN EMBOLECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K972572
510(k) Type
Traditional
Applicant
AMERICAN BIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/1998
Days to Decision
187 days
Submission Type
Summary

SINGLE LUMEN EMBOLECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K972572
510(k) Type
Traditional
Applicant
AMERICAN BIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/1998
Days to Decision
187 days
Submission Type
Summary