TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTER— 510(k) K862206

Name: FDA 510(k) clearance K862206
Creator: U.S. Food and Drug Administration
Published: 1986-08-04

Substantially Equivalent

Micromedic Systems

FDA 510(k) clearance K862206 for TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTER, Substantially Equivalent on 1986-08-04. Applicant: Micromedic Systems. Device class: 1.

Clearance details

Applicant: Micromedic Systems
Product code: Code JJJ
Device class: Class 1
Regulation: 21 CFR 862.2320
Advisory panel: Clinical Chemistry
Date received: 1986-06-10
Decision date: 1986-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Horsham, PA, US

Download summary PDF View on FDA.gov ↗

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