MOR
K-Number: K241897 · 2025-02-11
ApplicantMorari, Inc.
Decision Date2025-02-11
Product CodeQRC
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
MOR is the device name listed in this FDA 510(k) record. The listed applicant is Morari, Inc.. It received FDA 510(k) clearance on 2025-02-11 under 510(k) 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. The listed applicant is Morari, Inc.. The 510(k) number is K241897.
When did MOR receive FDA 510(k) clearance?
MOR received FDA 510(k) clearance on 2025-02-11, under 510(k) number K241897.
Who is the listed applicant for MOR?
The FDA 510(k) record lists Morari, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOR?
The FDA product code for MOR is QRC.
Related Devices (Code: QRC)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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