FDA 510(k) Applications Submitted by CORPAK MedSystems, Inc. a Division of Haylard Health
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K162110 | 07/29/2016 | CORGRIP NG/NI Tube Retention System | CORPAK MedSystems, Inc. a Division of Haylard Health |
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