Atomica Planner
K-Number: K230012 · 2023-02-02
ApplicantAtomica Technology, Inc.
Decision Date2023-02-02
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Atomica Planner is a medical device manufactured by Atomica Technology, Inc.. It received FDA 510(k) clearance on 2023-02-02 under approval number K230012. 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 Atomica Planner?
Atomica Planner is a medical device that received FDA 510(k) clearance on 2023-02-02. It is manufactured by Atomica Technology, Inc.. The 510(k) number is K230012.
When was Atomica Planner approved by the FDA?
Atomica Planner received FDA 510(k) clearance on 2023-02-02, under approval number K230012.
What company makes Atomica Planner?
Atomica Planner is manufactured by Atomica Technology, Inc..
What is the FDA product code for Atomica Planner?
The FDA product code for Atomica Planner 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.