SERUM, INORGANIC PHOSPHOROUS— 510(k) K790021

Name: FDA 510(k) clearance K790021
Creator: U.S. Food and Drug Administration
Published: 1979-02-15

Substantially Equivalent

Fisher Scientific Co., LLC

FDA 510(k) clearance K790021 for SERUM, INORGANIC PHOSPHOROUS, Substantially Equivalent on 1979-02-15. Applicant: Fisher Scientific Co., LLC. Device class: 1.

Clearance details

Applicant: Fisher Scientific Co., LLC
Product code: Code CEO
Device class: Class 1
Regulation: 21 CFR 862.1580
Advisory panel: Clinical Chemistry
Date received: 1979-01-03
Decision date: 1979-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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