FISHER DIAGNOSTICS HEMATALL III LAS REAGENT— 510(k) K874054

Name: FDA 510(k) clearance K874054
Creator: U.S. Food and Drug Administration
Published: 1987-10-20

Substantially Equivalent

Fisher Scientific Co., LLC

FDA 510(k) clearance K874054 for FISHER DIAGNOSTICS HEMATALL III LAS REAGENT, Substantially Equivalent on 1987-10-20. Applicant: Fisher Scientific Co., LLC. Device class: 1.

Clearance details

Applicant: Fisher Scientific Co., LLC
Product code: Code GGK
Device class: Class 1
Regulation: 21 CFR 864.8540
Advisory panel: Hematology
Date received: 1987-10-05
Decision date: 1987-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orangeburg, NY, US

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