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FDA 510(k)

Constellation (CON-001)

K-Number: K241280 · 2024-09-12

ApplicantQ Bio, Inc.
Decision Date2024-09-12
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Constellation (CON-001) is a medical device manufactured by Q Bio, Inc.. It received FDA 510(k) clearance on 2024-09-12 under approval number K241280. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Constellation (CON-001)?

Constellation (CON-001) is a medical device that received FDA 510(k) clearance on 2024-09-12. It is manufactured by Q Bio, Inc.. The 510(k) number is K241280.

When was Constellation (CON-001) approved by the FDA?

Constellation (CON-001) received FDA 510(k) clearance on 2024-09-12, under approval number K241280.

What company makes Constellation (CON-001)?

Constellation (CON-001) is manufactured by Q Bio, Inc..

What is the FDA product code for Constellation (CON-001)?

The FDA product code for Constellation (CON-001) is QIH.

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Official Source

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