IDEAL Ziploop
K-Number: K233552 · 2023-11-30
ApplicantRiverpoint Medical
Decision Date2023-11-30
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
IDEAL Ziploop is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2023-11-30 under approval number K233552. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the IDEAL Ziploop?
IDEAL Ziploop is a medical device that received FDA 510(k) clearance on 2023-11-30. It is manufactured by Riverpoint Medical. The 510(k) number is K233552.
When was IDEAL Ziploop approved by the FDA?
IDEAL Ziploop received FDA 510(k) clearance on 2023-11-30, under approval number K233552.
What company makes IDEAL Ziploop?
IDEAL Ziploop is manufactured by Riverpoint Medical.
What is the FDA product code for IDEAL Ziploop?
The FDA product code for IDEAL Ziploop is MBI.
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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.