Last synced on 18 April 2025 at 11:05 pm

CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120781
510(k) Type
Traditional
Applicant
FUJI SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2012
Days to Decision
147 days
Submission Type
Summary

CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120781
510(k) Type
Traditional
Applicant
FUJI SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2012
Days to Decision
147 days
Submission Type
Summary