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FDA 510(k)

CORGRIP NG/NI Tube Retention System

K-Number: K162110 · 2016-09-15

ApplicantCorpak Medsystems, Inc. A Division of Haylard Health
Decision Date2016-09-15
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

CORGRIP NG/NI Tube Retention System is a medical device manufactured by Corpak Medsystems, Inc. A Division of Haylard Health. It received FDA 510(k) clearance on 2016-09-15 under approval number K162110. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CORGRIP NG/NI Tube Retention System?

CORGRIP NG/NI Tube Retention System is a medical device that received FDA 510(k) clearance on 2016-09-15. It is manufactured by Corpak Medsystems, Inc. A Division of Haylard Health. The 510(k) number is K162110.

When was CORGRIP NG/NI Tube Retention System approved by the FDA?

CORGRIP NG/NI Tube Retention System received FDA 510(k) clearance on 2016-09-15, under approval number K162110.

What company makes CORGRIP NG/NI Tube Retention System?

CORGRIP NG/NI Tube Retention System is manufactured by Corpak Medsystems, Inc. A Division of Haylard Health.

What is the FDA product code for CORGRIP NG/NI Tube Retention System?

The FDA product code for CORGRIP NG/NI Tube Retention System is KNT.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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