Last synced on 14 November 2025 at 11:06 pm

ANGIOCOR SIDEHOLE INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K926293
510(k) Type
Traditional
Applicant
ANGIOCOR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
448 days
Submission Type
Statement

ANGIOCOR SIDEHOLE INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K926293
510(k) Type
Traditional
Applicant
ANGIOCOR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1994
Days to Decision
448 days
Submission Type
Statement