ANTICONVULSANTS II CALIBRATOR KIT— 510(k) K780734

Name: FDA 510(k) clearance K780734
Creator: U.S. Food and Drug Administration
Published: 1978-06-22

Substantially Equivalent

Vitek Systems, Inc.

FDA 510(k) clearance K780734 for ANTICONVULSANTS II CALIBRATOR KIT, Substantially Equivalent on 1978-06-22. Applicant: Vitek Systems, Inc.. Device class: 2.

Clearance details

Applicant: Vitek Systems, Inc.
Product code: Code DIY
Device class: Class 2
Regulation: 21 CFR 862.3380
Advisory panel: Clinical Toxicology
Date received: 1978-05-02
Decision date: 1978-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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