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THE AMPLATZ THROMBECTOMY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K954205
510(k) Type
Traditional
Applicant
MICROVENA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1996
Days to Decision
341 days
Submission Type
Summary

THE AMPLATZ THROMBECTOMY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K954205
510(k) Type
Traditional
Applicant
MICROVENA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1996
Days to Decision
341 days
Submission Type
Summary