DE-TOX TUBES A AND DE-TOX TUBES B— 510(k) K904326

Name: FDA 510(k) clearance K904326
Creator: U.S. Food and Drug Administration
Published: 1991-01-17

Substantially Equivalent

Dyna-Tek Industries

FDA 510(k) clearance K904326 for DE-TOX TUBES A AND DE-TOX TUBES B, Substantially Equivalent on 1991-01-17. Applicant: Dyna-Tek Industries. Device class: 1.

Clearance details

Applicant: Dyna-Tek Industries
Product code: Code DPA
Device class: Class 1
Regulation: 21 CFR 862.2270
Advisory panel: Clinical Chemistry
Date received: 1990-09-20
Decision date: 1991-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

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