Last synced on 14 November 2025 at 11:06 pm

LAPAROSCOPIC LASER FIBER DIVERTER

Page Type
Cleared 510(K)
510(k) Number
K912502
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1991
Days to Decision
50 days
Submission Type
Statement

LAPAROSCOPIC LASER FIBER DIVERTER

Page Type
Cleared 510(K)
510(k) Number
K912502
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1991
Days to Decision
50 days
Submission Type
Statement