Augmento
K-Number: K222781 · 2023-04-11
Decision Date2023-04-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Augmento is a medical device manufactured by Deeptek Medical Imaging Private Limited. It received FDA 510(k) clearance on 2023-04-11 under approval number K222781. 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 Augmento?
Augmento is a medical device that received FDA 510(k) clearance on 2023-04-11. It is manufactured by Deeptek Medical Imaging Private Limited. The 510(k) number is K222781.
When was Augmento approved by the FDA?
Augmento received FDA 510(k) clearance on 2023-04-11, under approval number K222781.
What company makes Augmento?
Augmento is manufactured by Deeptek Medical Imaging Private Limited.
What is the FDA product code for Augmento?
The FDA product code for Augmento 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.