AMPULED FLAME PHOTOMETER STANDARDS— 510(k) K810618

Name: FDA 510(k) clearance K810618
Creator: U.S. Food and Drug Administration
Published: 1981-03-31

Substantially Equivalent

United Diagnostics, Inc.

FDA 510(k) clearance K810618 for AMPULED FLAME PHOTOMETER STANDARDS, Substantially Equivalent on 1981-03-31. Applicant: United Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: United Diagnostics, Inc.
Product code: Code JIS
Device class: Class 2
Regulation: 21 CFR 862.1150
Advisory panel: Clinical Chemistry
Date received: 1981-03-09
Decision date: 1981-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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