VINT
K-Number: K240385 · 2024-10-15
ApplicantMediimg Corporation
Decision Date2024-10-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
VINT is a medical device manufactured by Mediimg Corporation. It received FDA 510(k) clearance on 2024-10-15 under approval number K240385. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VINT?
VINT is a medical device that received FDA 510(k) clearance on 2024-10-15. It is manufactured by Mediimg Corporation. The 510(k) number is K240385.
When was VINT approved by the FDA?
VINT received FDA 510(k) clearance on 2024-10-15, under approval number K240385.
What company makes VINT?
VINT is manufactured by Mediimg Corporation.
What is the FDA product code for VINT?
The FDA product code for VINT is LLZ.
Related Devices (Code: LLZ)
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.