Nutrifit
K-Number: K243361 · 2024-12-19
ApplicantVygon USA
Decision Date2024-12-19
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Nutrifit is a medical device manufactured by Vygon USA. It received FDA 510(k) clearance on 2024-12-19 under approval number K243361. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nutrifit?
Nutrifit is a medical device that received FDA 510(k) clearance on 2024-12-19. It is manufactured by Vygon USA. The 510(k) number is K243361.
When was Nutrifit approved by the FDA?
Nutrifit received FDA 510(k) clearance on 2024-12-19, under approval number K243361.
What company makes Nutrifit?
Nutrifit is manufactured by Vygon USA.
What is the FDA product code for Nutrifit?
The FDA product code for Nutrifit is FPD.
Other Devices by Vygon USA
Related Devices (Code: FPD)
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.