sensiLift
K-Number: K170499 · 2017-06-15
Device Summary
Frequently Asked Questions
What is the sensiLift?
sensiLift is a medical device that received FDA 510(k) clearance on 2017-06-15. The listed applicant is El Global Trade, Ltd.. The 510(k) number is K170499.
When did sensiLift receive FDA 510(k) clearance?
sensiLift received FDA 510(k) clearance on 2017-06-15, under 510(k) number K170499.
Who is the listed applicant for sensiLift?
The FDA 510(k) record lists El Global Trade, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for sensiLift?
The FDA product code for sensiLift is PAY.
Other records listing El Global Trade, Ltd. 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.
Related Devices (Code: PAY)
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.
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.