Last synced on 14 November 2025 at 11:06 pm

PERIPHERAL DILATATION ANGIOPLASTY-CATH

Page Type
Cleared 510(K)
510(k) Number
K834429
510(k) Type
Traditional
Applicant
AMERICAN EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1984
Days to Decision
239 days

PERIPHERAL DILATATION ANGIOPLASTY-CATH

Page Type
Cleared 510(K)
510(k) Number
K834429
510(k) Type
Traditional
Applicant
AMERICAN EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1984
Days to Decision
239 days