MICROHEMATOCRIT ROTOR— 510(k) K930415

Name: FDA 510(k) clearance K930415
Creator: U.S. Food and Drug Administration
Published: 1993-03-23

Substantially Equivalent

Fisher Scientific Co., LLC

FDA 510(k) clearance K930415 for MICROHEMATOCRIT ROTOR, Substantially Equivalent on 1993-03-23. Applicant: Fisher Scientific Co., LLC. Device class: 2.

Clearance details

Applicant: Fisher Scientific Co., LLC
Product code: Code GKG
Device class: Class 2
Regulation: 21 CFR 864.6400
Advisory panel: Hematology
Date received: 1993-01-26
Decision date: 1993-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pittsburgh, PA, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.