Clarify DL
K-Number: K241350 · 2025-01-03
Decision Date2025-01-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Clarify DL is a medical device manufactured by Ge Medical Systems Israel, Functional Imaging. It received FDA 510(k) clearance on 2025-01-03 under approval number K241350. 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 Clarify DL?
Clarify DL is a medical device that received FDA 510(k) clearance on 2025-01-03. It is manufactured by Ge Medical Systems Israel, Functional Imaging. The 510(k) number is K241350.
When was Clarify DL approved by the FDA?
Clarify DL received FDA 510(k) clearance on 2025-01-03, under approval number K241350.
What company makes Clarify DL?
Clarify DL is manufactured by Ge Medical Systems Israel, Functional Imaging.
What is the FDA product code for Clarify DL?
The FDA product code for Clarify DL is LLZ.
Other Devices by Ge Medical Systems Israel, Functional Imaging
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.