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CORTRAK ENTERAL ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K113351
510(k) Type
Special
Applicant
CORPAK MEDSYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2012
Days to Decision
57 days
Submission Type
Statement

CORTRAK ENTERAL ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K113351
510(k) Type
Special
Applicant
CORPAK MEDSYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2012
Days to Decision
57 days
Submission Type
Statement