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CORPAK PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K882867
510(k) Type
Traditional
Applicant
CORPAK CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1988
Days to Decision
72 days

CORPAK PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE

Page Type
Cleared 510(K)
510(k) Number
K882867
510(k) Type
Traditional
Applicant
CORPAK CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1988
Days to Decision
72 days