ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III— 510(k) K931907

Name: FDA 510(k) clearance K931907
Creator: U.S. Food and Drug Administration
Published: 1993-09-29

Substantially Equivalent

Anthos Labtec Instruments

FDA 510(k) clearance K931907 for ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III, Substantially Equivalent on 1993-09-29. Applicant: Anthos Labtec Instruments. Device class: 1.

Clearance details

Applicant: Anthos Labtec Instruments
Product code: Code JJQ
Device class: Class 1
Regulation: 21 CFR 862.2300
Advisory panel: Clinical Chemistry
Date received: 1993-04-15
Decision date: 1993-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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