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CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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