LIO

Device, Specimen Collection

Product code

LIO

Device name

Device, Specimen Collection

Device class

Class 1

21 CFR

21 CFR 866.2900

Medical specialty

Microbiology

Marketing pathway

510(K)

Flag

Third-party review eligible

510(k) clearances (last 3 years)

1

Summaries archived here

1 (direct download)

510(k) clearances (all years, FDA)

63 (all years; only the last 3 years are listed here)

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2024-03-27.

1 summaries are archived here for direct download.