SPRYTIE, MODELS ST001, ST002 AND ST003— 510(k) K092530

Name: FDA 510(k) clearance K092530
Creator: U.S. Food and Drug Administration
Published: 2010-04-02

Substantially Equivalent

Russell B. Walther

FDA 510(k) clearance K092530 for SPRYTIE, MODELS ST001, ST002 AND ST003, Substantially Equivalent on 2010-04-02. Applicant: Russell B. Walther. Device class: 2.

Clearance details

Applicant: Russell B. Walther
Product code: Code DZK
Device class: Class 2
Regulation: 21 CFR 872.4880
Advisory panel: Dental
Date received: 2009-08-18
Decision date: 2010-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

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