PHA-1 PROGRAMMABLE HEMATOLOGY ANALYZ— 510(k) K834372

Name: FDA 510(k) clearance K834372
Creator: U.S. Food and Drug Administration
Published: 1984-02-10

Substantially Equivalent

Diagnostic Technology, Inc.

FDA 510(k) clearance K834372 for PHA-1 PROGRAMMABLE HEMATOLOGY ANALYZ, Substantially Equivalent on 1984-02-10. Applicant: Diagnostic Technology, Inc.. Device class: 2.

Clearance details

Applicant: Diagnostic Technology, Inc.
Product code: Code GKL
Device class: Class 2
Regulation: 21 CFR 864.5200
Advisory panel: Hematology
Date received: 1983-12-01
Decision date: 1984-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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