Leica FL400— 510(k) DEN180024

Unknown

Leica Microsystems (Schweiz) AG

FDA 510(k) clearance DEN180024 for Leica FL400, Unknown on 2019-03-28. Applicant: Leica Microsystems (Schweiz) AG. Device class: 2.

Clearance details

Applicant: Leica Microsystems (Schweiz) AG
Product code: Code QFX
Device class: Class 2
Regulation: 21 CFR 882.4950
Advisory panel: Neurology
Date received: 2018-04-27
Decision date: 2019-03-28
Decision: Unknown
Clearance type: Direct
Location: Heerbrugg, CH

View on FDA.gov ↗

Recent devices under product code QFX

K251286 — Affirm 4002026-01-21
K240215 — BLUE 400; BLUE 400 S2024-06-28
K232567 — Myriad SPECTRA Light Source2024-03-14
K211346 — BLUE 4002022-07-22

More clearances from Leica Microsystems (Schweiz) AG

Data sourced from openFDA. This site is unofficial and independent of the FDA.