ELVI 828 DIGICLOT MULTISCAN— 510(k) K902614

Name: FDA 510(k) clearance K902614
Creator: U.S. Food and Drug Administration
Published: 1990-11-08

Substantially Equivalent

Logos Scientific, Inc.

FDA 510(k) clearance K902614 for ELVI 828 DIGICLOT MULTISCAN, Substantially Equivalent on 1990-11-08. Applicant: Logos Scientific, Inc.. Device class: 2.

Clearance details

Applicant: Logos Scientific, Inc.
Product code: Code KQG
Device class: Class 2
Regulation: 21 CFR 864.5400
Advisory panel: Hematology
Date received: 1990-06-13
Decision date: 1990-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Henderson, NV, US

Download summary PDF View on FDA.gov ↗

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