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FDA 510(k)

Bone Suppression Software

K-Number: K240281 · 2024-05-31

ApplicantKonica Minolta, Inc.
Decision Date2024-05-31
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Bone Suppression Software is a medical device manufactured by Konica Minolta, Inc.. It received FDA 510(k) clearance on 2024-05-31 under approval number K240281. 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 Bone Suppression Software?

Bone Suppression Software is a medical device that received FDA 510(k) clearance on 2024-05-31. It is manufactured by Konica Minolta, Inc.. The 510(k) number is K240281.

When was Bone Suppression Software approved by the FDA?

Bone Suppression Software received FDA 510(k) clearance on 2024-05-31, under approval number K240281.

What company makes Bone Suppression Software?

Bone Suppression Software is manufactured by Konica Minolta, Inc..

What is the FDA product code for Bone Suppression Software?

The FDA product code for Bone Suppression Software is LLZ.

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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.

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