Decision Date2023-03-24
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Starly pad is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Xingyuanli Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-03-24 under 510(k) number K221589. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Starly pad?
Starly pad is a medical device that received FDA 510(k) clearance on 2023-03-24. The listed applicant is Shenzhen Xingyuanli Technology Co., Ltd.. The 510(k) number is K221589.
When did Starly pad receive FDA 510(k) clearance?
Starly pad received FDA 510(k) clearance on 2023-03-24, under 510(k) number K221589.
Who is the listed applicant for Starly pad?
The FDA 510(k) record lists Shenzhen Xingyuanli Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Starly pad?
The FDA product code for Starly pad is GXY.
Related Devices (Code: GXY)
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.
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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.