COUNTER CHECK, H001, H002, H003— 510(k) K790025

Name: FDA 510(k) clearance K790025
Creator: U.S. Food and Drug Administration
Published: 1979-01-17

Substantially Equivalent

Diagnostic Technology, Inc.

FDA 510(k) clearance K790025 for COUNTER CHECK, H001, H002, H003, Substantially Equivalent on 1979-01-17. Applicant: Diagnostic Technology, Inc.. Device class: 2.

Clearance details

Applicant: Diagnostic Technology, Inc.
Product code: Code KSF
Device class: Class 2
Regulation: 21 CFR 864.9650
Advisory panel: Hematology
Date received: 1979-01-03
Decision date: 1979-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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