Sensilift Pro (ST300XXYYZZZ)
K-Number: K250341 · 2026-01-06
ApplicantEl Global Trade, Ltd.
Decision Date2026-01-06
Product CodePAY
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Sensilift Pro (ST300XXYYZZZ) is a medical device manufactured by El Global Trade, Ltd.. It received FDA 510(k) clearance on 2026-01-06 under approval number K250341. The device is classified under product code PAY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Sensilift Pro (ST300XXYYZZZ)?
Sensilift Pro (ST300XXYYZZZ) is a medical device that received FDA 510(k) clearance on 2026-01-06. It is manufactured by El Global Trade, Ltd.. The 510(k) number is K250341.
When was Sensilift Pro (ST300XXYYZZZ) approved by the FDA?
Sensilift Pro (ST300XXYYZZZ) received FDA 510(k) clearance on 2026-01-06, under approval number K250341.
What company makes Sensilift Pro (ST300XXYYZZZ)?
Sensilift Pro (ST300XXYYZZZ) is manufactured by El Global Trade, Ltd..
What is the FDA product code for Sensilift Pro (ST300XXYYZZZ)?
The FDA product code for Sensilift Pro (ST300XXYYZZZ) is PAY.
Other Devices by El Global Trade, Ltd.
Related Devices (Code: PAY)
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.