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DISTENTION INSTRUMENT, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K934134
510(k) Type
Traditional
Applicant
ORIGIN MEDSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/1993
Days to Decision
48 days
Submission Type
Statement

DISTENTION INSTRUMENT, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K934134
510(k) Type
Traditional
Applicant
ORIGIN MEDSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/1993
Days to Decision
48 days
Submission Type
Statement