Daylight
K-Number: K233872 · 2024-08-30
ApplicantBig Health, Inc.
Decision Date2024-08-30
Product CodeSCP
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Daylight is a medical device manufactured by Big Health, Inc.. It received FDA 510(k) clearance on 2024-08-30 under approval 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. It is manufactured by Big Health, Inc.. The 510(k) number is K233872.
When was Daylight approved by the FDA?
Daylight received FDA 510(k) clearance on 2024-08-30, under approval number K233872.
What company makes Daylight?
Daylight is manufactured by Big Health, Inc..
What is the FDA product code for Daylight?
The FDA product code for Daylight is SCP.
Other Devices by Big Health, Inc.
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.