CephNinja
K-Number: K241819 · 2025-01-23
ApplicantCyncronus, LLC
Decision Date2025-01-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
CephNinja is a medical device manufactured by Cyncronus, LLC. It received FDA 510(k) clearance on 2025-01-23 under approval number K241819. 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 CephNinja?
CephNinja is a medical device that received FDA 510(k) clearance on 2025-01-23. It is manufactured by Cyncronus, LLC. The 510(k) number is K241819.
When was CephNinja approved by the FDA?
CephNinja received FDA 510(k) clearance on 2025-01-23, under approval number K241819.
What company makes CephNinja?
CephNinja is manufactured by Cyncronus, LLC.
What is the FDA product code for CephNinja?
The FDA product code for CephNinja 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.