Last synced on 14 November 2025 at 11:06 pm

CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP

Page Type
Cleared 510(K)
510(k) Number
K911243
510(k) Type
Traditional
Applicant
NORTHGATE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/1991
Days to Decision
90 days

CHOLANGIOCATH AND ATRAUMATIC BOWEL CLAMP

Page Type
Cleared 510(K)
510(k) Number
K911243
510(k) Type
Traditional
Applicant
NORTHGATE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/1991
Days to Decision
90 days