Last synced on 14 November 2025 at 11:06 pm

ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K821816
510(k) Type
Traditional
Applicant
MEDI-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1982
Days to Decision
64 days

ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K821816
510(k) Type
Traditional
Applicant
MEDI-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1982
Days to Decision
64 days