LEUKOCYTE VOL. ANALYSIS APPARATUS— 510(k) K802208

Substantially Equivalent

Coulter Electronics, Inc.

FDA 510(k) clearance K802208 for LEUKOCYTE VOL. ANALYSIS APPARATUS, Substantially Equivalent on 1980-09-17. Applicant: Coulter Electronics, Inc..

Clearance details

Applicant: Coulter Electronics, Inc.
Product code: Code GKL
Advisory panel: Hematology
Date received: 1980-09-11
Decision date: 1980-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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