Last synced on 14 November 2025 at 11:06 pm

GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K822243
510(k) Type
Traditional
Applicant
INTERVENTIONAL MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1982
Days to Decision
28 days

GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K822243
510(k) Type
Traditional
Applicant
INTERVENTIONAL MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/1982
Days to Decision
28 days