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PG Pro Microcatheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192625
510(k) Type
Traditional
Applicant
MicroVention, Inc., A Terumo Group Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2019
Days to Decision
59 days
Submission Type
Summary

PG Pro Microcatheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192625
510(k) Type
Traditional
Applicant
MicroVention, Inc., A Terumo Group Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2019
Days to Decision
59 days
Submission Type
Summary