WAND PLUS— 510(k) K992819

Substantially Equivalent

Spintech, Inc.

FDA 510(k) clearance K992819 for WAND PLUS, Substantially Equivalent on 2000-05-11. Applicant: Spintech, Inc.. Device class: 2.

Clearance details

Applicant: Spintech, Inc.
Product code: Code EJI
Device class: Class 2
Regulation: 21 CFR 872.6770
Advisory panel: Dental
Date received: 1999-08-20
Decision date: 2000-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.