TriMed Ripcord Device
K-Number: K220650 · 2022-06-01
ApplicantTriMed, Inc.
Decision Date2022-06-01
Product CodeHTN
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
TriMed Ripcord Device is a medical device manufactured by TriMed, Inc.. It received FDA 510(k) clearance on 2022-06-01 under approval number K220650. The device is classified under product code HTN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TriMed Ripcord Device?
TriMed Ripcord Device is a medical device that received FDA 510(k) clearance on 2022-06-01. It is manufactured by TriMed, Inc.. The 510(k) number is K220650.
When was TriMed Ripcord Device approved by the FDA?
TriMed Ripcord Device received FDA 510(k) clearance on 2022-06-01, under approval number K220650.
What company makes TriMed Ripcord Device?
TriMed Ripcord Device is manufactured by TriMed, Inc..
What is the FDA product code for TriMed Ripcord Device?
The FDA product code for TriMed Ripcord Device is HTN.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.