Last synced on 25 January 2026 at 3:41 am

SCIMED PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILAT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850075
510(k) Type
Traditional
Applicant
SCIMED LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1985
Days to Decision
91 days

SCIMED PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILAT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850075
510(k) Type
Traditional
Applicant
SCIMED LIFE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1985
Days to Decision
91 days