MICRO HAEMATOCRIT CENTRIFUGE— 510(k) K960491

Name: FDA 510(k) clearance K960491
Creator: U.S. Food and Drug Administration
Published: 1996-10-18

Substantially Equivalent

Hawksley & Sons , Ltd.

FDA 510(k) clearance K960491 for MICRO HAEMATOCRIT CENTRIFUGE, Substantially Equivalent on 1996-10-18. Applicant: Hawksley & Sons , Ltd.. Device class: 2.

Clearance details

Applicant: Hawksley & Sons , Ltd.
Product code: Code CKG
Device class: Class 2
Regulation: 21 CFR 862.1025
Advisory panel: Clinical Chemistry
Date received: 1996-02-01
Decision date: 1996-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lancing, West Sussex, GB

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