MICRO-HEMATOCRIT CENTRIFUGE 335/336— 510(k) K823558

Name: FDA 510(k) clearance K823558
Creator: U.S. Food and Drug Administration
Published: 1983-01-21

Substantially Equivalent

Fisher Scientific Co., LLC

FDA 510(k) clearance K823558 for MICRO-HEMATOCRIT CENTRIFUGE 335/336, Substantially Equivalent on 1983-01-21. Applicant: Fisher Scientific Co., LLC. Device class: 2.

Clearance details

Applicant: Fisher Scientific Co., LLC
Product code: Code JPI
Device class: Class 2
Regulation: 21 CFR 864.6400
Advisory panel: Hematology
Date received: 1982-12-02
Decision date: 1983-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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