Last synced on 9 May 2025 at 11:05 pm

SCIMED VIPER 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
K944815
510(k) Type
Traditional
Applicant
SCIMED LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1994
Days to Decision
46 days
Submission Type
Summary

SCIMED VIPER 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
K944815
510(k) Type
Traditional
Applicant
SCIMED LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1994
Days to Decision
46 days
Submission Type
Summary