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FDA 510(k)

Coconut Hybrid

K-Number: K242162 · 2024-09-19

Decision Date2024-09-19
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Coconut Hybrid is a medical device manufactured by Good Clean Love, Inc.. It received FDA 510(k) clearance on 2024-09-19 under approval number K242162. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Coconut Hybrid?

Coconut Hybrid is a medical device that received FDA 510(k) clearance on 2024-09-19. It is manufactured by Good Clean Love, Inc.. The 510(k) number is K242162.

When was Coconut Hybrid approved by the FDA?

Coconut Hybrid received FDA 510(k) clearance on 2024-09-19, under approval number K242162.

What company makes Coconut Hybrid?

Coconut Hybrid is manufactured by Good Clean Love, Inc..

What is the FDA product code for Coconut Hybrid?

The FDA product code for Coconut Hybrid is NUC.

Other Devices by Good Clean Love, Inc.

Related Devices (Code: NUC)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.