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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 the device name listed in this FDA 510(k) record. The listed applicant is Uplevity, Inc.. It received FDA 510(k) clearance on 2018-08-30 under 510(k) 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. The listed applicant is Uplevity, Inc.. The 510(k) number is K180888.

When did LYFT receive FDA 510(k) clearance?

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

Who is the listed applicant for LYFT?

The FDA 510(k) record lists Uplevity, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LYFT?

The FDA product code for LYFT is OLP.

Related Devices (Code: OLP)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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