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FDA 510(k)

LYFT

K-Number: K180888 · 2018-08-30

ApplicantUplevity, Inc.
Decision Date2018-08-30
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LYFT is a medical device manufactured by Uplevity, Inc.. It received FDA 510(k) clearance on 2018-08-30 under approval number K180888. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYFT?

LYFT is a medical device that received FDA 510(k) clearance on 2018-08-30. It is manufactured by Uplevity, Inc.. The 510(k) number is K180888.

When was LYFT approved by the FDA?

LYFT received FDA 510(k) clearance on 2018-08-30, under approval number K180888.

What company makes LYFT?

LYFT is manufactured by Uplevity, Inc..

What is the FDA product code for LYFT?

The FDA product code for LYFT is OLP.

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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.

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