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FDA 510(k)

Daylight

K-Number: K233872 · 2024-08-30

ApplicantBig Health, Inc.
Decision Date2024-08-30
Product CodeSCP
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Daylight is the device name listed in this FDA 510(k) record. The listed applicant is Big Health, Inc.. It received FDA 510(k) clearance on 2024-08-30 under 510(k) number K233872. The device is classified under product code SCP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Daylight?

Daylight is a medical device that received FDA 510(k) clearance on 2024-08-30. The listed applicant is Big Health, Inc.. The 510(k) number is K233872.

When did Daylight receive FDA 510(k) clearance?

Daylight received FDA 510(k) clearance on 2024-08-30, under 510(k) number K233872.

Who is the listed applicant for Daylight?

The FDA 510(k) record lists Big Health, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Daylight?

The FDA product code for Daylight is SCP.

Other records listing Big Health, Inc. as applicant

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.

K233577Sleepio®

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.

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