SYSMEX R-1000 AUTOMATED RETICULOCYTE ANALYZER— 510(k) K894539

Substantially Equivalent

Toa Medical Electronics USA, Inc.

FDA 510(k) clearance K894539 for SYSMEX R-1000 AUTOMATED RETICULOCYTE ANALYZER, Substantially Equivalent on 1989-09-26. Applicant: Toa Medical Electronics USA, Inc..

Clearance details

Applicant: Toa Medical Electronics USA, Inc.
Product code: Code GKL
Advisory panel: Hematology
Date received: 1989-07-20
Decision date: 1989-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Alamitos, CA, US

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