MOR
K-Number: K241897 · 2025-02-11
ApplicantMorari, Inc.
Decision Date2025-02-11
Product CodeQRC
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
MOR is a medical device manufactured by Morari, Inc.. It received FDA 510(k) clearance on 2025-02-11 under approval number K241897. The device is classified under product code QRC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MOR?
MOR is a medical device that received FDA 510(k) clearance on 2025-02-11. It is manufactured by Morari, Inc.. The 510(k) number is K241897.
When was MOR approved by the FDA?
MOR received FDA 510(k) clearance on 2025-02-11, under approval number K241897.
What company makes MOR?
MOR is manufactured by Morari, Inc..
What is the FDA product code for MOR?
The FDA product code for MOR is QRC.
Related Devices (Code: QRC)
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.