MLX MICROTITER PLATE LUMINOMETER— 510(k) K962265

Name: FDA 510(k) clearance K962265
Creator: U.S. Food and Drug Administration
Published: 1996-07-25

Substantially Equivalent

Dynatech Laboratories, Inc.

FDA 510(k) clearance K962265 for MLX MICROTITER PLATE LUMINOMETER, Substantially Equivalent on 1996-07-25. Applicant: Dynatech Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Dynatech Laboratories, Inc.
Product code: Code JSE
Device class: Class 1
Regulation: 21 CFR 866.2320
Advisory panel: Microbiology
Date received: 1996-06-12
Decision date: 1996-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chantilly, VA, US

Download summary PDF View on FDA.gov ↗

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