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BAXTER PERCUTANEOUS MECHANICAL THROMBECTOMY (PMT) DEVICE, MODELS PMT0606FD AND PMT1206FD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993816
510(k) Type
Traditional
Applicant
BAXTER EDWARDS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2000
Days to Decision
176 days
Submission Type
Summary

BAXTER PERCUTANEOUS MECHANICAL THROMBECTOMY (PMT) DEVICE, MODELS PMT0606FD AND PMT1206FD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993816
510(k) Type
Traditional
Applicant
BAXTER EDWARDS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2000
Days to Decision
176 days
Submission Type
Summary