Last synced on 14 November 2025 at 11:06 pm

SCIMED PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILAT

Page Type
Cleared 510(K)
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)
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