CORGRIP NG/NI Tube Retention System
K-Number: K162110 · 2016-09-15
Device Summary
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. The listed applicant is Corpak Medsystems, Inc. A Division of Haylard Health. The 510(k) number is K162110.
When did CORGRIP NG/NI Tube Retention System receive FDA 510(k) clearance?
CORGRIP NG/NI Tube Retention System received FDA 510(k) clearance on 2016-09-15, under 510(k) number K162110.
Who is the listed applicant for CORGRIP NG/NI Tube Retention System?
The FDA 510(k) record lists Corpak Medsystems, Inc. A Division of Haylard Health as the applicant. This does not by itself establish the device manufacturer.
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.
Related Devices (Code: KNT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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