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PREPERITONEAL DISTENTION BALLOON SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K935426
510(k) Type
Traditional
Applicant
ORIGIN MEDSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1994
Days to Decision
77 days
Submission Type
Statement

PREPERITONEAL DISTENTION BALLOON SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K935426
510(k) Type
Traditional
Applicant
ORIGIN MEDSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1994
Days to Decision
77 days
Submission Type
Statement