MICROLITE MICROTITER PLATE LUMINOMETER ML3000— 510(k) K923456

Name: FDA 510(k) clearance K923456
Creator: U.S. Food and Drug Administration
Published: 1992-10-13

Substantially Equivalent

Dynatech Laboratories, Inc.

FDA 510(k) clearance K923456 for MICROLITE MICROTITER PLATE LUMINOMETER ML3000, Substantially Equivalent on 1992-10-13. Applicant: Dynatech Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Dynatech Laboratories, Inc.
Product code: Code JJQ
Device class: Class 1
Regulation: 21 CFR 862.2300
Advisory panel: Clinical Chemistry
Date received: 1992-07-14
Decision date: 1992-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chantilly, VA, US

Download summary PDF View on FDA.gov ↗

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