FDA 510(k)

LYFT

K号: K180888 · 2018-08-30

决定日期2018-08-30

产品代码OLP

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决定实质等同

器械摘要

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.

常见问题

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.

相关器械（代码：OLP）

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