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CORGRIP NG/NI Tube Retention System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162110
510(k) Type
Traditional
Applicant
CORPAK MedSystems, Inc. a Division of Haylard Health
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
9/15/2016
Days to Decision
48 days
Submission Type
Summary