Last synced on 2 December 2022 at 11:04 pm

CORTRAK ENTERAL ACCESS DEVICE

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