Last synced on 18 April 2025 at 11:05 pm

BOBBY Balloon Guide Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193607
510(k) Type
Traditional
Applicant
MicroVention, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2020
Days to Decision
208 days
Submission Type
Summary

BOBBY Balloon Guide Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193607
510(k) Type
Traditional
Applicant
MicroVention, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/2020
Days to Decision
208 days
Submission Type
Summary