EDENTEC MODEL 3710 I DIGITAL PRINTER— 510(k) K921819

Name: FDA 510(k) clearance K921819
Creator: U.S. Food and Drug Administration
Published: 1993-10-22

Substantially Equivalent

Edentec Corp.

FDA 510(k) clearance K921819 for EDENTEC MODEL 3710 I DIGITAL PRINTER, Substantially Equivalent on 1993-10-22. Applicant: Edentec Corp.. Device class: 2.

Clearance details

Applicant: Edentec Corp.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1992-04-15
Decision date: 1993-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eden Prairie, MN, US

Download summary PDF View on FDA.gov ↗

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