INTEGRA REAGENT CASSETTE FOR HEMOGLOBIN ALC— 510(k) K990992

Name: FDA 510(k) clearance K990992
Creator: U.S. Food and Drug Administration
Published: 1999-09-30

Substantially Equivalent

Roche Diagnostics Corp.

FDA 510(k) clearance K990992 for INTEGRA REAGENT CASSETTE FOR HEMOGLOBIN ALC, Substantially Equivalent on 1999-09-30. Applicant: Roche Diagnostics Corp.. Device class: 2.

Clearance details

Applicant: Roche Diagnostics Corp.
Product code: Code LCP
Device class: Class 2
Regulation: 21 CFR 864.7470
Advisory panel: Hematology
Date received: 1999-03-24
Decision date: 1999-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

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