MICROMEDIC AUTOMATIC DILUTER— 510(k) K800606

Name: FDA 510(k) clearance K800606
Creator: U.S. Food and Drug Administration
Published: 1980-04-16

Substantially Equivalent

Micromedic Systems

FDA 510(k) clearance K800606 for MICROMEDIC AUTOMATIC DILUTER, Substantially Equivalent on 1980-04-16. Applicant: Micromedic Systems. Device class: 1.

Clearance details

Applicant: Micromedic Systems
Product code: Code JQW
Device class: Class 1
Regulation: 21 CFR 862.2750
Advisory panel: Clinical Chemistry
Date received: 1980-03-17
Decision date: 1980-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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