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PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052757
510(k) Type
Special
Applicant
BIOTRONIK AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2005
Days to Decision
28 days
Submission Type
Summary

PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052757
510(k) Type
Special
Applicant
BIOTRONIK AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2005
Days to Decision
28 days
Submission Type
Summary