OLYMPUS REPLY UREA NITROGEN REAGENT— 510(k) K931745

Name: FDA 510(k) clearance K931745
Creator: U.S. Food and Drug Administration
Published: 1993-08-19

Substantially Equivalent

Olympus Corp.

FDA 510(k) clearance K931745 for OLYMPUS REPLY UREA NITROGEN REAGENT, Substantially Equivalent on 1993-08-19. Applicant: Olympus Corp.. Device class: 2.

Clearance details

Applicant: Olympus Corp.
Product code: Code CDQ
Device class: Class 2
Regulation: 21 CFR 862.1770
Advisory panel: Clinical Chemistry
Date received: 1993-04-05
Decision date: 1993-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Success, NY, US

Download summary PDF View on FDA.gov ↗

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