RipCord
K-Number: K251134 · 2025-07-11
ApplicantTriMed, Inc.
Decision Date2025-07-11
Product CodeHTN
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
RipCord is a medical device manufactured by TriMed, Inc.. It received FDA 510(k) clearance on 2025-07-11 under approval number K251134. 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 RipCord?
RipCord is a medical device that received FDA 510(k) clearance on 2025-07-11. It is manufactured by TriMed, Inc.. The 510(k) number is K251134.
When was RipCord approved by the FDA?
RipCord received FDA 510(k) clearance on 2025-07-11, under approval number K251134.
What company makes RipCord?
RipCord is manufactured by TriMed, Inc..
What is the FDA product code for RipCord?
The FDA product code for RipCord 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.