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FASCIAL CLOSURE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K931522
510(k) Type
Traditional
Applicant
ORIGIN MEDSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1994
Days to Decision
314 days
Submission Type
Statement

FASCIAL CLOSURE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K931522
510(k) Type
Traditional
Applicant
ORIGIN MEDSYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1994
Days to Decision
314 days
Submission Type
Statement