SERUMAX (AUTOMATED SERUM CENTRIFUGATION & STATION)— 510(k) K893400

Name: FDA 510(k) clearance K893400
Creator: U.S. Food and Drug Administration
Published: 1989-06-23

Substantially Equivalent

Medical Robotics

FDA 510(k) clearance K893400 for SERUMAX (AUTOMATED SERUM CENTRIFUGATION & STATION), Substantially Equivalent on 1989-06-23. Applicant: Medical Robotics. Device class: 1.

Clearance details

Applicant: Medical Robotics
Product code: Code JQW
Device class: Class 1
Regulation: 21 CFR 862.2750
Advisory panel: Clinical Chemistry
Date received: 1989-05-01
Decision date: 1989-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lexington, KY, US

Download summary PDF View on FDA.gov ↗

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