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PREPERITONEAL DISTENTION BALLOON SYSTEMS (MODIFICATION)

Page Type
Cleared 510(K)
510(k) Number
K953561
510(k) Type
Traditional
Applicant
ORIGIN MEDSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1995
Days to Decision
28 days
Submission Type
Summary

PREPERITONEAL DISTENTION BALLOON SYSTEMS (MODIFICATION)

Page Type
Cleared 510(K)
510(k) Number
K953561
510(k) Type
Traditional
Applicant
ORIGIN MEDSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1995
Days to Decision
28 days
Submission Type
Summary