RISTOCETIN— 510(k) K900792

Name: FDA 510(k) clearance K900792
Creator: U.S. Food and Drug Administration
Published: 1990-03-27

Substantially Equivalent

Medical Diagnostic Technologies, Inc.

FDA 510(k) clearance K900792 for RISTOCETIN, Substantially Equivalent on 1990-03-27. Applicant: Medical Diagnostic Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Medical Diagnostic Technologies, Inc.
Product code: Product code GHR
Device class: Class 2
Regulation: 21 CFR 864.5700
Advisory panel: Hematology
Date received: 1990-02-20
Decision date: 1990-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ventura, CA, US

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