WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS— 510(k) K913089

Name: FDA 510(k) clearance K913089
Creator: U.S. Food and Drug Administration
Published: 1992-04-21

Substantially Equivalent

Wilde-USA, Inc.

FDA 510(k) clearance K913089 for WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS, Substantially Equivalent on 1992-04-21. Applicant: Wilde-USA, Inc.. Device class: 2.

Clearance details

Applicant: Wilde-USA, Inc.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 1991-07-12
Decision date: 1992-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naperville, IL, US

Download summary PDF View on FDA.gov ↗

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