pNOVUS 21 Microcatheter
K-Number: K242420 · 2024-11-12
ApplicantPhenox, Ltd.
Decision Date2024-11-12
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
pNOVUS 21 Microcatheter is a medical device manufactured by Phenox, Ltd.. It received FDA 510(k) clearance on 2024-11-12 under approval number K242420. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the pNOVUS 21 Microcatheter?
pNOVUS 21 Microcatheter is a medical device that received FDA 510(k) clearance on 2024-11-12. It is manufactured by Phenox, Ltd.. The 510(k) number is K242420.
When was pNOVUS 21 Microcatheter approved by the FDA?
pNOVUS 21 Microcatheter received FDA 510(k) clearance on 2024-11-12, under approval number K242420.
What company makes pNOVUS 21 Microcatheter?
pNOVUS 21 Microcatheter is manufactured by Phenox, Ltd..
What is the FDA product code for pNOVUS 21 Microcatheter?
The FDA product code for pNOVUS 21 Microcatheter is DQO.
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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.