IL TEST PHOSPHORUS— 510(k) K931361

Name: FDA 510(k) clearance K931361
Creator: U.S. Food and Drug Administration
Published: 1993-05-11

Substantially Equivalent

Instrumentation Laboratory CO

FDA 510(k) clearance K931361 for IL TEST PHOSPHORUS, Substantially Equivalent on 1993-05-11. Applicant: Instrumentation Laboratory CO. Device class: 1.

Clearance details

Applicant: Instrumentation Laboratory CO
Product code: Code CEO
Device class: Class 1
Regulation: 21 CFR 862.1580
Advisory panel: Clinical Chemistry
Date received: 1993-03-17
Decision date: 1993-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lexington, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.