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CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE

Page Type
Cleared 510(K)
510(k) Number
K935512
510(k) Type
Traditional
Applicant
CORPAK CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1996
Days to Decision
1017 days
Submission Type
Statement

CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE

Page Type
Cleared 510(K)
510(k) Number
K935512
510(k) Type
Traditional
Applicant
CORPAK CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/1996
Days to Decision
1017 days
Submission Type
Statement